Excess production of ADRENAL CORTEX HORMONES such as ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. Hyperadrenal syndromes include CUSHING SYNDROME; HYPERALDOSTERONISM; and VIRILISM.
A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM.
Tumors or cancers of the ADRENAL CORTEX.
The striated muscle groups which move the LARYNX as a whole or its parts, such as altering tension of the VOCAL CORDS, or size of the slit (RIMA GLOTTIDIS).
Difficulty and/or pain in PHONATION or speaking.
A variety of techniques used to help individuals utilize their voice for various purposes and with minimal use of muscle energy.
Pathological processes that affect voice production, usually involving VOCAL CORDS and the LARYNGEAL MUCOSA. Voice disorders can be caused by organic (anatomical), or functional (emotional or psychological) factors leading to DYSPHONIA; APHONIA; and defects in VOICE QUALITY, loudness, and pitch.
The process of producing vocal sounds by means of VOCAL CORDS vibrating in an expiratory blast of air.
A benign neoplasm of the ADRENAL CORTEX. It is characterized by a well-defined nodular lesion, usually less than 2.5 cm. Most adrenocortical adenomas are nonfunctional. The functional ones are yellow and contain LIPIDS. Depending on the cell type or cortical zone involved, they may produce ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE.
The outer layer of the adrenal gland. It is derived from MESODERM and comprised of three zones (outer ZONA GLOMERULOSA, middle ZONA FASCICULATA, and inner ZONA RETICULARIS) with each producing various steroids preferentially, such as ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and ANDROSTENEDIONE. Adrenal cortex function is regulated by pituitary ADRENOCORTICOTROPIN.
That component of SPEECH which gives the primary distinction to a given speaker's VOICE when pitch and loudness are excluded. It involves both phonatory and resonatory characteristics. Some of the descriptions of voice quality are harshness, breathiness and nasality.
FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome.
A pair of cone-shaped elastic mucous membrane projecting from the laryngeal wall and forming a narrow slit between them. Each contains a thickened free edge (vocal ligament) extending from the THYROID CARTILAGE to the ARYTENOID CARTILAGE, and a VOCAL MUSCLE that shortens or relaxes the vocal cord to control sound production.

Stress-level cortisol treatment impairs inhibitory control of behavior in monkeys. (1/78)

Most studies of cortisol-induced cognitive impairments have focused on hippocampal-dependent memory. This study investigates a different aspect of cognition in a randomized placebo-controlled experiment with monkeys that were treated with cortisol according to a protocol that simulates a prolonged stress response. Young adult and older adult monkeys were assigned randomly to placebo or chronic treatment with cortisol in a 2 x 2 factorial design (n = 8 monkeys per condition). Inhibitory control of behavior was assessed with a test shown previously in primates to reflect prefrontal cortical dysfunction. Failure to inhibit a specific goal-directed response was evident more often in older adults. Treatment with cortisol increased this propensity in both older and young adult monkeys. Age-related differences in response inhibition were consistent across blocks of repeated test trials, but the treatment effects were clearly expressed only after prolonged exposure to cortisol. Aspects of performance that did not require inhibition were not altered by age or treatment with cortisol, which concurs with effects on response inhibition rather than nonspecific changes in behavior. These findings lend support to related reports that cortisol-induced disruptions in prefrontal dopamine neurotransmission may contribute to deficits in response inhibition and play a role in cognitive impairments associated with endogenous hypercortisolism in humans.  (+info)

Glucocorticoid and mineralocorticoid resistance/hypersensitivity syndromes. (2/78)

Glucocorticoids and mineralocorticoids regulate diverse functions important to maintain central nervous system, cardiovascular, metabolic, and immune homeostasis. The actions of these hormones are mediated by their specific intracellular receptors: the glucocorticoid (GR) and mineralocorticoid (MR) receptors. Pathologic conditions associated with changes of tissue sensitivity to these hormones have been described. The syndrome of familial glucocorticoid resistance is characterized by hypercortisolism without Cushing's syndrome stigmata. The molecular defects of four kindreds and one sporadic case have been elucidated as inactivating mutations in the ligand-binding domain of GR. Two cases developed glucocorticoid resistance at the heterozygous state. In these patients, mutant receptors possessed transdominant negative activity upon the wild type receptor. Insensitivity to mineralocorticoids (which may also be caused by loss of function mutations of the MR gene) was found in one sporadic case and four autosomal dominant cases of Pseudohypoaldosteronism type 1. These included two frameshift mutations and a premature termination codon in exon 2, leading to gene products lacking the entire DNA- and ligand-binding domains, and a single base-pair deletion in the intron-5 splice donor site. Tissue hypersensitivity to glucocorticoids was recently hypothesized in patients with Human Immunodeficiency Virus (HIV) type-1 infection via the accessory proteins Vpr and Tat which enhance GR transactivation. Since HIV-1 long terminal repeat (LTR) and glucocorticoid-responsive promoters use the same set of coactivators, these proteins may stimulate HIV-1-LTR and glucocorticoid-inducible genes concurrently. The former may directly stimulate viral proliferation, while the latter may indirectly enhance viral propagation by suppressing the host immune system through glucocorticoid-mediated mechanisms.  (+info)

Uptake ratio of (19-1311) cholesterol by adrenal glands as observed by a scintigraphic method. (3/78)

The adrenal scintigram was performed after administration of [19-131I] cholesterol. A high/low ratio of both adrenal glands was calculated to evaluate whether there is a difference between the left and right sides in adrenal diseases. During scanning, information was stored in a 64 X 64 matrix and then punched out on a computer compatible paper tape. This paper tape was processed with a small digital computer. The areas of interest were selected over adrenal glands. The computer decided mean counts per unit area. After subtraction of background counts, a high/low ratio of adrenal gland was calculated. In five patients with Cushing's syndrome due to bilateral hyperplasia, a high/low ratio ranged from 1.0 to 2.0. In four patients with primary aldosteronism due to adenoma, a high/low ratio ranged from 1.33 to 4.0. This method may be useful to differentiate bilateral hyperplasia from unilateral adrenocortical adenoma.  (+info)

From open to laparoscopic adrenalectomy: a review of 16-year experience. (4/78)

OBJECTIVE: To review the experience with adrenal surgery which was associated with significant morbidity and notable mortality in the past, although laparoscopic approach is beginning to be accepted as the procedure of choice. METHODS: The indications and results of adrenalectomy in 104 patients (36 men, 68 women) over the past 16 years were reviewed. Any potential improvement of surgical results over time was analyzed. RESULTS: Ninety-three patients (89%) had functional problems while malignancy was present in 11 patients (11%). Anterior approach was employed in 27 patients, posterior in 56, lateral in 10, and laparoscopic in 11. One patient required conversion from laparoscopic to anterior approach. No operative mortality was seen, but the morbidity occurred in 16.7%. Complication rate decreased significantly in this study period (1981-1990 versus 1991-1996, 22% versus 5%; P = 0.02). Laparoscopic adrenalectomy was successfully performed for 59% of the patients requiring adrenalectomy recently, compared to 68% of posterior adrenalectomy in the past. CONCLUSIONS: Adrenal surgery is a safe procedure, associated with acceptable morbidity, which has decreased over time. Laparoscopic adrenalectomy is becoming the preferred approach for the majority of patients requiring adrenalectomy.  (+info)

Parathyroid hormone secretion in chronic human endogenous hypercortisolism. (5/78)

Osteoporosis is a common manifestation of Cushing's syndrome, but the mechanisms responsible for this abnormality have not been defined. With the objective of analyzing parathyroid hormone (PTH) secretion in chronic hypercortisolism (CH), we evaluated 11 healthy subjects and 8 patients with CH, 6 with Cushing's disease and 2 with adrenal adenoma. These volunteers were submitted to tests of PTH stimulation through hypocalcemia (EDTA), PTH suppression through hypercalcemia (iv and oral calcium), and evaluation of bone mineral density (BMD) by DEXA. During the test of PTH stimulation, the calcium and magnesium concentrations of the normal and CH groups were similar. Patients with CH showed an increased PTH response to the hypocalcemic stimulus compared to controls. PTH values were significantly higher in the CH group at 70 (17.5 +/- 3.5 vs 10.2 +/- 1.3 pmol/l, P = 0.04), and 120 min (26.1 +/- 5.9 vs 11.3 +/- 1.9 pmol/l, P = 0.008) of EDTA infusion. The area under the curve for PTH during EDTA infusion was also significantly higher in patients with CH than in normal subjects (1867 +/- 453 and 805 +/- 148 pmol l(-1) 2 h(-1), P = 0.02). During the test of PTH suppression, calcium, magnesium and PTH levels of the patients with hypercortisolism and controls were similar. BMD was decreased in patients with hypercortisolism in the spine (0.977 +/- 0.052 vs 1.205 +/- 0.038 g/cm2 in controls, P<0.01). In conclusion, our results show that subjects with CH present decreased bone mass mainly in trabecular bone. The use of dynamic tests permitted the detection of increased PTH secretion in response to a hypocalcemic stimulus in CH patients that may probably be involved in the occurrence of osteoporosis in this state.  (+info)

Arterial lesions in repeatedly bred spontaneously hypertensive rats. (6/78)

Repeatedly bred male and female rats of many strains develop hyperglycemia, hyperlipidemia, hypertension, and arteriosclerosis spontaneously. The intensity of their arterial disease and related metabolic derangements appear to be related to their reproductive activity. Repeatedly bred spontaneously hypertensive rats (SHR) were found to have severe hypertension, hyperglycemia, hyperlipidemia, elevated creatine phosphokinase (CPK), serum glutamic oxaloacetic and glutamic pyruvic transaminase (SGOT, SGPT), and lactic dehydrogenase (LDH), as well as high circulating corticosterone levels. Despite these atherogenic metabolic derangements and their severe hypertension, the breeder SHR did not develop the severe, generalized arteriosclerosis found in other strains of breeder rats. Instead, the arterial lesions, consisting of intimal hyalinization and fibrosis, medial hypertrophy, and occlusion of the lumen, were found only in male breeder SHR and were confined to the intratubular arteries of the testes. It is suggested that the severe hypertension, genetic influences, or differences in hypothalamic-pituitary-adrenal-gonadal function in breeder SHR may not have been conducive to the development of arteriosclerosis in this particular strain of rats.  (+info)

Osteoporosis is more prevalent in adrenal than in pituitary Cushing's syndrome. (7/78)

Osteoporosis is the most common complication of Cushing's syndrome. We retrospectively examined the prevalence and risk factors for osteoporosis in 42 female patients with Cushing's syndrome. Osteoporosis and atraumatic fractures were assessed by bone mineral density of the lumbar vertebral spine (L2-L4) using dual energy X-ray absorptiometry (DXA) and X-ray examination. The prevalence of osteoporosis and fracture were 54.8% and 21.4%, respectively. The prevalence of osteoporosis (69.6% vs. 37.8%) and atraumatic bone fracture (26.1% vs. 15.8%) were significantly higher in patients with adrenal Cushing's than in those with pituitary Cushing's. AP and lateral BMD was significantly higher in patients with pituitary origin than in those with adrenal origin. Among several variables examined by multiple logistic regression, the etiology of Cushing's syndrome (adrenal vs. pituitary origin) was a significant factor affecting the prevalence of osteoporosis. Neither age, body mass index, duration of amenorrhea, nor extent of hypercortisolism were significant factors in this analysis. Plasma DHEA-S and urinary 17-KS excretion were significantly higher in pituitary Cushing's than in adrenal Cushing's. The present study shows that the prevalence of osteoporosis in patients with Cushing's syndrome is influenced by its etiology. A factor associated with pituitary Cushing's syndrome, such as adrenal androgen, may protect these patients from glucocorticoid-induced osteoporosis.  (+info)

CARCINOMA OF LUNG WITH ADRENAL HYPERFUNCTION AND HYPERCALCEMIA TREATED BY PARATHYROIDECTOMY. (8/78)

A case of severe hypercalcemia secondary to carcinoma of the lung is described in which hypokalemic alkalosis, renal failure and pancreatitis were also present. The relative importance of the few bone metastases found at autopsy is considered, and a probable endocrine-like effect of the tumour in the development of the hypercalcemia is postulated. Treatment of the hypercalcemia included administration of corticosteroids and disodium EDTA, peritoneal dialysis and subtotal parathyroidectomy; the most effective of these was peritoneal dialysis. Subtotal parathyroidectomy failed to produce a further decrease in serum calcium values. The occurrence of hypokalemic alkalosis in the presence of increased adrenocortical function and its relationship to the carcinoma of the lung are discussed. The possibility that this neoplasm produced two factors which caused systemic effects ordinarily associated with the function of endocrine glands must be considered.  (+info)

Adrenocortical hyperfunction, also known as Cushing's syndrome, is a condition characterized by the overproduction of cortisol hormone from the adrenal glands. The adrenal glands are located on top of the kidneys and are responsible for producing several essential hormones, including cortisol. Cortisol helps regulate metabolism, blood pressure, and the body's response to stress.

In Adrenocortical hyperfunction, the adrenal glands produce too much cortisol, leading to a range of symptoms such as weight gain, particularly around the trunk and face, thinning of the skin, easy bruising, muscle weakness, mood changes, and high blood pressure. The condition can be caused by several factors, including tumors in the pituitary gland or adrenal glands, long-term use of corticosteroid medications, or genetic disorders that affect the adrenal glands.

Treatment for Adrenocortical hyperfunction depends on the underlying cause of the condition and may include surgery to remove tumors, medication to reduce cortisol production, or radiation therapy. It is essential to diagnose and treat this condition promptly, as long-term exposure to high levels of cortisol can lead to serious health complications such as diabetes, osteoporosis, and heart disease.

Adrenocortical carcinoma (ACC) is a rare cancer that develops in the outer layer of the adrenal gland, known as the adrenal cortex. The adrenal glands are small hormone-producing glands located on top of each kidney. They produce important hormones such as cortisol, aldosterone, and sex steroids.

ACC is a malignant tumor that can invade surrounding tissues and organs and may metastasize (spread) to distant parts of the body. Symptoms of ACC depend on the size and location of the tumor and whether it produces excess hormones. Common symptoms include abdominal pain, a mass in the abdomen, weight loss, and weakness. Excessive production of hormones can lead to additional symptoms such as high blood pressure, Cushing's syndrome, virilization (excessive masculinization), or feminization.

The exact cause of ACC is not known, but genetic factors, exposure to certain chemicals, and radiation therapy may increase the risk of developing this cancer. Treatment options for ACC include surgery, chemotherapy, radiation therapy, and targeted therapy. The prognosis for ACC varies depending on the stage and extent of the disease at diagnosis, as well as the patient's overall health.

Adrenal cortex neoplasms refer to abnormal growths (tumors) in the adrenal gland's outer layer, known as the adrenal cortex. These neoplasms can be benign or malignant (cancerous). Benign tumors are called adrenal adenomas, while cancerous tumors are called adrenocortical carcinomas.

Adrenal cortex neoplasms can produce various hormones, leading to different clinical presentations. For instance, they may cause Cushing's syndrome (characterized by excessive cortisol production), Conn's syndrome (caused by aldosterone excess), or virilization (due to androgen excess). Some tumors may not produce any hormones and are discovered incidentally during imaging studies for unrelated conditions.

The diagnosis of adrenal cortex neoplasms typically involves a combination of imaging techniques, such as CT or MRI scans, and hormonal assessments to determine if the tumor is functional or non-functional. In some cases, a biopsy may be necessary to confirm the diagnosis and differentiate between benign and malignant tumors. Treatment options depend on the type, size, location, and hormonal activity of the neoplasm and may include surgical excision, radiation therapy, chemotherapy, or a combination of these approaches.

The laryngeal muscles are a group of skeletal muscles located in the larynx, also known as the voice box. These muscles play a crucial role in breathing, swallowing, and producing sounds for speech. They include:

1. Cricothyroid muscle: This muscle helps to tense the vocal cords and adjust their pitch during phonation (voice production). It is the only laryngeal muscle that is not innervated by the recurrent laryngeal nerve. Instead, it is supplied by the external branch of the superior laryngeal nerve.
2. Posterior cricoarytenoid muscle: This muscle is primarily responsible for abducting (opening) the vocal cords during breathing and speaking. It is the only muscle that can abduct the vocal cords.
3. Lateral cricoarytenoid muscle: This muscle adducts (closes) the vocal cords during phonation, swallowing, and coughing.
4. Transverse arytenoid muscle: This muscle also contributes to adduction of the vocal cords, working together with the lateral cricoarytenoid muscle. It also helps to relax and lengthen the vocal cords during quiet breathing.
5. Oblique arytenoid muscle: This muscle is involved in adducting, rotating, and shortening the vocal cords. It works together with the transverse arytenoid muscle to provide fine adjustments for voice production.
6. Thyroarytenoid muscle (Vocalis): This muscle forms the main body of the vocal cord and is responsible for its vibration during phonation. The vocalis portion of the muscle helps control pitch and tension in the vocal cords.

These muscles work together to enable various functions of the larynx, such as breathing, swallowing, and speaking.

Dysphonia is a medical term that refers to difficulty or discomfort in producing sounds or speaking, often characterized by hoarseness, roughness, breathiness, strain, or weakness in the voice. It can be caused by various conditions such as vocal fold nodules, polyps, inflammation, neurological disorders, or injuries to the vocal cords. Dysphonia can affect people of all ages and may impact their ability to communicate effectively, causing social, professional, and emotional challenges. Treatment for dysphonia depends on the underlying cause and may include voice therapy, medication, surgery, or lifestyle modifications.

"Voice training" is not a term that has a specific medical definition in the field of otolaryngology (ear, nose, and throat medicine) or speech-language pathology. However, voice training generally refers to the process of developing and improving one's vocal skills through various exercises and techniques. This can include training in breath control, pitch, volume, resonance, articulation, and interpretation, among other aspects of vocal production. Voice training is often used to help individuals with voice disorders or professionals such as singers and actors to optimize their vocal abilities. In a medical context, voice training may be recommended or overseen by a speech-language pathologist as part of the treatment plan for a voice disorder.

Voice disorders are conditions that affect the quality, pitch, or volume of a person's voice. These disorders can result from damage to or abnormalities in the vocal cords, which are the small bands of muscle located in the larynx (voice box) that vibrate to produce sound.

There are several types of voice disorders, including:

1. Vocal cord dysfunction: This occurs when the vocal cords do not open and close properly, resulting in a weak or breathy voice.
2. Vocal cord nodules: These are small growths that form on the vocal cords as a result of excessive use or misuse of the voice, such as from shouting or singing too loudly.
3. Vocal cord polyps: These are similar to nodules but are usually larger and can cause more significant changes in the voice.
4. Laryngitis: This is an inflammation of the vocal cords that can result from a viral infection, overuse, or exposure to irritants such as smoke.
5. Muscle tension dysphonia: This occurs when the muscles around the larynx become tense and constricted, leading to voice changes.
6. Paradoxical vocal fold movement: This is a condition in which the vocal cords close when they should be open, causing breathing difficulties and a weak or breathy voice.
7. Spasmodic dysphonia: This is a neurological disorder that causes involuntary spasms of the vocal cords, resulting in voice breaks and difficulty speaking.

Voice disorders can cause significant impairment in communication, social interactions, and quality of life. Treatment may include voice therapy, medication, or surgery, depending on the underlying cause of the disorder.

Phonation is the process of sound production in speech, singing, or crying. It involves the vibration of the vocal folds (also known as the vocal cords) in the larynx, which is located in the neck. When air from the lungs passes through the vibrating vocal folds, it causes them to vibrate and produce sound waves. These sound waves are then shaped into speech sounds by the articulatory structures of the mouth, nose, and throat.

Phonation is a critical component of human communication and is used in various forms of verbal expression, such as speaking, singing, and shouting. It requires precise control of the muscles that regulate the tension, mass, and length of the vocal folds, as well as the air pressure and flow from the lungs. Dysfunction in phonation can result in voice disorders, such as hoarseness, breathiness, or loss of voice.

An adrenocortical adenoma is a benign tumor that arises from the cells of the adrenal cortex, which is the outer layer of the adrenal gland. These tumors can produce and release various hormones, such as cortisol, aldosterone, or androgens, depending on the type of cells they originate from.

Most adrenocortical adenomas are nonfunctioning, meaning that they do not secrete excess hormones and may not cause any symptoms. However, some functioning adenomas can produce excessive amounts of hormones, leading to a variety of clinical manifestations. For example:

* Cortisol-secreting adenomas can result in Cushing's syndrome, characterized by weight gain, muscle wasting, thin skin, easy bruising, and mood changes.
* Aldosterone-producing adenomas can cause Conn's syndrome, marked by hypertension (high blood pressure), hypokalemia (low potassium levels), and metabolic alkalosis.
* Androgen-secreting adenomas may lead to hirsutism (excessive hair growth) or virilization (development of male secondary sexual characteristics) in women.

The diagnosis of an adrenocortical adenoma typically involves imaging tests, such as CT or MRI scans, and hormonal evaluations to determine if the tumor is functioning or not. Treatment usually consists of surgical removal of the tumor, especially if it is causing hormonal imbalances or growing in size.

The adrenal cortex is the outer portion of the adrenal gland, which is located on top of the kidneys. It plays a crucial role in producing hormones that are essential for various bodily functions. The adrenal cortex is divided into three zones:

1. Zona glomerulosa: This outermost zone produces mineralocorticoids, primarily aldosterone. Aldosterone helps regulate sodium and potassium balance and thus influences blood pressure by controlling the amount of fluid in the body.
2. Zona fasciculata: The middle layer is responsible for producing glucocorticoids, with cortisol being the most important one. Cortisol regulates metabolism, helps manage stress responses, and has anti-inflammatory properties. It also plays a role in blood sugar regulation and maintaining the body's response to injury and illness.
3. Zona reticularis: The innermost zone produces androgens, primarily dehydroepiandrosterone (DHEA) and its sulfate form (DHEAS). These androgens are weak compared to those produced by the gonads (ovaries or testes), but they can be converted into more potent androgens or estrogens in peripheral tissues.

Disorders related to the adrenal cortex can lead to hormonal imbalances, affecting various bodily functions. Examples include Addison's disease (insufficient adrenal cortical hormone production) and Cushing's syndrome (excessive glucocorticoid levels).

Voice quality, in the context of medicine and particularly in otolaryngology (ear, nose, and throat medicine), refers to the characteristic sound of an individual's voice that can be influenced by various factors. These factors include the vocal fold vibration, respiratory support, articulation, and any underlying medical conditions.

A change in voice quality might indicate a problem with the vocal folds or surrounding structures, neurological issues affecting the nerves that control vocal fold movement, or other medical conditions. Examples of terms used to describe voice quality include breathy, hoarse, rough, strained, or tense. A detailed analysis of voice quality is often part of a speech-language pathologist's assessment and can help in diagnosing and managing various voice disorders.

Fibrous Dysplasia, Polyostotic is a rare genetic disorder that affects the bone tissue. It is characterized by the replacement of normal bone tissue with fibrous (scar-like) tissue, leading to weak and fragile bones that are prone to fractures and deformities. The term "polyostotic" refers to the involvement of multiple bones in the body.

In this condition, there is an abnormal development of the bone during fetal growth or early childhood due to a mutation in the GNAS gene. This results in the formation of fibrous tissue instead of normal bone tissue, leading to the characteristic features of Fibrous Dysplasia, Polyostotic.

The symptoms of this condition can vary widely depending on the severity and location of the affected bones. Common symptoms include:

* Bone pain and tenderness
* Bone deformities (such as bowing of the legs)
* Increased risk of fractures
* Skin pigmentation changes (cafe-au-lait spots)
* Hearing loss or other hearing problems (if the skull is affected)

Fibrous Dysplasia, Polyostotic can also be associated with endocrine disorders such as precocious puberty and hyperthyroidism. Treatment typically involves a combination of medications to manage pain and prevent fractures, as well as surgical intervention to correct bone deformities or stabilize fractures.

Vocal cords, also known as vocal folds, are specialized bands of muscle, membrane, and connective tissue located within the larynx (voice box). They are essential for speech, singing, and other sounds produced by the human voice. The vocal cords vibrate when air from the lungs is passed through them, creating sound waves that vary in pitch and volume based on the tension, length, and mass of the vocal cords. These sound waves are then further modified by the resonance chambers of the throat, nose, and mouth to produce speech and other vocalizations.

... is a condition where there is an overexpression of products of the adrenal cortex. When cortisol ... "Growth in disorders of adrenal hyperfunction". Pediatric endocrinology reviews: PER. 1 Suppl 3: 484-489. ISSN 1565-4753. ...
Lada G, Gyódi E, Gláz E (1977). "HLA antigens in patients with adrenocortical hyperfunction". Acta Med Acad Sci Hung. 34 (4): ... Among these were coeliac disease, autoimmune active chronic hepatitis, myasthenia gravis, Adrenocortical hyperfunction- ...
... familial Adrenal cancer Adrenal disorder Adrenal gland hyperfunction Adrenal gland hypofunction Adrenal hyperplasia Adrenal ... X-linked Adrenal incidentaloma Adrenal insufficiency Adrenal macropolyadenomatosis Adrenal medulla neoplasm Adrenocortical ...
Adrenal disorders may cause hyperfunction or hypofunction, and may be congenital or acquired. The adrenal gland produces ... or may be inactive Adrenocortical carcinoma, cancer of the adrenal cortex Adrenal incidentaloma, an adrenal tumor (of any type ...
Most notably she discovered with her husband Webb E. Haymaker that Cushing's disease is caused by hyper function of the adrenal ... adreno-cortical thyroid hormone or ACTH) in 1934. Evelyn Anderson was born in Willmar, Minnesota, to Swedish immigrants parents ...
Endocrine gland hyperfunction/hypersecretion (leading to hormone excess) Tumours (benign or malignant) of endocrine glands ... acute adrenocortical insufficiency, phaeochromocytoma crisis, hypercalcemic crisis, thyroid storm, myxoedema coma and pituitary ...
Hyperfunction can occur as a result of hypersecretion, loss of suppression, hyperplastic or neoplastic change, or ... Pohorecky LA, Wurtman RJ (March 1971). "Adrenocortical control of epinephrine synthesis". Pharmacological Reviews. 23 (1): 1-35 ...
Adrenocortical hyperfunction is a condition where there is an overexpression of products of the adrenal cortex. When cortisol ... "Growth in disorders of adrenal hyperfunction". Pediatric endocrinology reviews: PER. 1 Suppl 3: 484-489. ISSN 1565-4753. ...
"Adrenocortical Hyperfunction (Cushing Disease, Cushing Syndrome)." Quick Medical Diagnosis & Treatment Pediatrics Hay, Jr WW, ... Adrenocortical Hyperfunction (Cushing Disease, Cushing Syndrome). In: Hay, Jr WW, Levin MJ, Deterding RR, Abzug MJ. Hay, Jr W.W ... Adrenocortical hyperfunction (cushing disease, cushing syndrome). Hay, Jr WW, Levin MJ, Deterding RR, Abzug MJ. Hay, Jr W.W ... If possible, surgical removal is indicated in all cases of primary adrenal hyperfunction due to tumor ...
Adrenocortical hyperfunction syndromes 46. Hypothyreosis 47. Gastrointestinal bleeding 48. Intoxication by addictive substances ...
... autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty). Other endocrine syndromes may be present ... Cushing syndrome associated with MAS is predominantly due to adrenocortical hyperfunction. Most of these cases have been ... Autonomous endocrine hyperfunction - The most common form of autonomous endocrine hyperfunction in this syndrome is precocious ... Testicular or ovarian hyperfunction is the most common abnormality. Laboratory studies that may be helpful include the ...
... autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty). Other endocrine syndromes may be present ... Cushing syndrome associated with MAS is predominantly due to adrenocortical hyperfunction. Most of these cases have been ... Autonomous endocrine hyperfunction - The most common form of autonomous endocrine hyperfunction in this syndrome is precocious ... Testicular or ovarian hyperfunction is the most common abnormality. Laboratory studies that may be helpful include the ...
The diurnal rhythm of the HPA axis is lost in Cushings disease, a syndrome of adrenocortical hyperfunction characterized by ... Adrenocortical insufficiency may result from too rapid withdrawal of corticosteroids and may be minimized by gradual reduction ... Drug-induced secondary adrenocortical insufficiency may be minimized by gradual reduction of dosage. This type of relative ... Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be ...
The diurnal rhythm of the HPA axis is lost in Cushings disease, a syndrome of adrenocortical hyperfunction characterized by ... Drug-induced secondary adrenocortical insufficiency may be minimized by gradual reduction of dosage. This type of relative ... Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be ... Exogenous corticosteroids suppress adrenocortical activity the least, when given at the time of maximal activity (am). ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenal Gland Hyperfunction. Adrenocortical Hyperfunction. Adrenal Gland Hypofunction. Adrenal Insufficiency. Bartters Disease ...
Adrenocortical hyperfunction can be caused by a variety of factors, including:. 1. Cushings syndrome: This is a rare hormonal ... Adrenocortical hyperfunction refers to an excessive or abnormal increase in the production of hormones by the adrenal glands, ... Treatment options for adrenocortical hyperfunction depend on the underlying cause of the condition and may include:. 1. ... Symptoms of adrenocortical hyperfunction may include:. 1. Weight gain and central obesity. 2. Increased appetite and food ...
Adrenocortical Hyperfunction (Hyperadrenalism). Synthesize and secrete 3 major steroid hormones. Mineralocorticoids: ... Adrenocortical Adenoma:. -Most cortical adenomas do not cause hyperfunction and are usually encountered incidentally ... Adrenocortical tumors may be benign or malignant.. -Adrenocortical adenoma  encapsulated, expansile, yellow tumors, lipid-rich ... Unilateral adrenocortical neoplasm: Benign (Adenoma) or Malignant (Carcinoma). *The secretion of ectopic ACTH by nonendocrine ...
Adrenocortical hyperfunction, 4.1.17.. Aggression against oneself, 6.5.F.. Aggression against others, 6.5.F.. Aggressive ... Thyroid gland hyperfunction, 2.1.4.. Thyroid gland hypofunction, 2.1.4.. Thyroid gland, 2.1.4.. Thyroid hormone deficiency, 2.1 ...
Diagnostic testing of adrenocortical hyperfunction. 14. Cerebral Edema associated with primary or metastatic brain tumor, ... Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be ... Drug-induced secondary adrenocortical insufficiency may result from too rapid withdrawal of corticosteroids and may be ... Acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be ...
... primary adrenocortical insufficiency, adrenocortical hyperfunction or sensitivity to proteins of porcine origins. ...
... autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty). Other endocrine syndromes may be present ... Cushing syndrome associated with MAS is predominantly due to adrenocortical hyperfunction. Most of these cases have been ... Autonomous endocrine hyperfunction - The most common form of autonomous endocrine hyperfunction in this syndrome is precocious ... Testicular or ovarian hyperfunction is the most common abnormality. Laboratory studies that may be helpful include the ...
... autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty). Other endocrine syndromes may be present ... Cushing syndrome associated with MAS is predominantly due to adrenocortical hyperfunction. Most of these cases have been ... Autonomous endocrine hyperfunction - The most common form of autonomous endocrine hyperfunction in this syndrome is precocious ... Testicular or ovarian hyperfunction is the most common abnormality. Laboratory studies that may be helpful include the ...
... primary adrenocortical insufficiency, adrenocortical hyperfunction or sensitivity to proteins of porcine origins. ...
An adrenal cortex that makes too much of the hormones cortisol and aldosterone (adrenocortical hyperfunction) ... Adrenal glands that do not make enough of the hormone cortisol (primary adrenocortical insufficiency) or ...
The mechanism of acrodynia may also involve adrenocortical hyperfunction, sympathetic vasomotor dysfunction, and catecholamine ...
Diagnostic testing of adrenocortical hyperfunction, trichinosis with neurologic or myocardial involvement, tuberculous ... Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; may be used in ...
  • McCune-Albright syndrome (MAS) consists of at least two of the following three features: (1) polyostotic fibrous dysplasia (PFD), (2) café-au-lait skin pigmentation (see the image below), and (3) autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty ). (medscape.com)
  • Introduction: McCune-Albright syndrome (MAS) consists of at least two of the following three conditions: polyostotic fibrous dysplasia (PFD), café-au-lait skin pigmentation and autonomous endocrine hyperfunction. (endocrine-abstracts.org)
  • The most common form of autonomous endocrine hyperfunction is precocious puberty, but other syndromes may be present, including acromegaly, hyperthyroidism, and Cushing syndrome. (endocrine-abstracts.org)
  • A complete medical history and physical examination are important in the evaluation of MAS, especially with an eye toward finding apparent endocrine hyperfunction and skeletal deformities. (medscape.com)
  • Problems with the adrenals can be due to either a change in function, such as Hypofunction (decreased production of adrenal hormones) or Hyperfunction (increased production of adrenal hormones), or to the development of a non-functional lump in the gland (incidentaloma). (endocrinesurgeon.co.uk)
  • Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. (nih.gov)
  • Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. (nih.gov)
  • Introduction: Adrenocortical carcinoma (ACC) is a rare and aggressive tumor, with a poor prognosis and median survival of 3-4 years. (endocrine-abstracts.org)
  • Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful. (nih.gov)
  • During 2002-2017, the most common incident adrenal gland disorder among male and female service members was adrenal insufficiency and the least common was adrenomedullary hyperfunction. (health.mil)
  • In both sexes, overall rates of other disorders of adrenal gland and Cushing's syndrome were lower than for adrenal insufficiency but higher than for hyperaldosteronism, adrenogenital disorders, and adrenomedullary hyperfunction. (health.mil)
  • Most adrenal deficiency syndromes affect output of all adrenocortical hormones. (msdmanuals.com)
  • Primary or secondary adrenocortical insufficiency, congenital adrenal hyperplasia, hypercalcemia associated with cancer and nonsuppurative thyroiditis. (com.bd)
  • A rare disease marked by deficient secretion of adrenocortical hormones (such as cortisol) that is characterized by fatigue, muscle weakness, weight loss, low blood pressure, irritability or depression, and brownish pigmentation of the skin, and is caused by progressive destruction of the adrenal glands (as by an autoimmune response or infection). (mhmedical.com)
  • With or without lab testing, if symptoms indicate adrenocortical deficiency, a low dose therapeutic trial of cortisol for several weeks may prove both informative and helpful. (digitalnaturopath.com)
  • Adrenocortical adenoma  encapsulated, expansile, yellow tumors, lipid-rich cells, adjacent adrenal cortex and contralateral adrenal glands are atrophic b/c of suppression of endogenous ACTH by high cortisol levels. (docsbay.net)
  • BACKGROUND: Primary aldosteronism is frequently caused by an adrenocortical aldosterone-producing adenoma (APA) carrying a somatic mutation that drives aldosterone overproduction. (bvsalud.org)
  • Finally, APA-like cell subpopulations-negative for CYP11B2 gene expression-were identified in adrenocortical tissue adjacent to APAs suggesting the existence of tumor precursor states. (bvsalud.org)
  • Because of this, it is suitable for the treatment of acute disorders responsive to adrenocortical steroid therapy. (medlibrary.org)
  • The mechanism of acrodynia may also involve adrenocortical hyperfunction, sympathetic vasomotor dysfunction, and catecholamine dysfunction. (statpearls.com)
  • Acthar is contraindicated in patients with scleroderma, osteoporosis, systemic fungal infections, ocular herpes simplex, recent surgery, history of or the presence of a peptic ulcer, congestive heart failure, uncontrolled hypertension, primary adrenocortical insufficiency, adrenocortical hyperfunction or sensitivity to proteins of porcine origins. (mallinckrodt.com)
  • Increased plasma Cl--concentrations (hyperchloremia) occur with dehydration, renal tubular acidosis, acute renal failure, in adrenocortical hyperfunction , salicylate intoxication and metabolic acidosis associated with prolonged diarrhoea and loss of sodium bicarbonate. (vitroscient.com)
  • Hyperfunction can result from either excessive production of a hormone from the gland itself, or excessive stimulation of the gland. (endocrinesurgeon.co.uk)
  • Testicular or ovarian hyperfunction is the most common abnormality. (medscape.com)
  • Shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected. (nih.gov)
  • Adrenocortical insufficiency (AI) occurs mainly in paediatric age and it can be the first manifestation of the disease in some cas. (endocrine-abstracts.org)
  • Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful. (nih.gov)
  • Shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected. (nih.gov)
  • Purified Cortrophin Gel is contraindicated in patients with primary adrenocortical insufficiency or adrenocortical hyperfunction. (nih.gov)
  • Primary or secondary adrenocortical insufficiency, congenital adrenal hyperplasia, hypercalcemia associated with cancer and nonsuppurative thyroiditis. (com.bd)
  • During 2002-2017, the most common incident adrenal gland disorder among male and female service members was adrenal insufficiency and the least common was adrenomedullary hyperfunction. (health.mil)
  • In both sexes, overall rates of other disorders of adrenal gland and Cushing's syndrome were lower than for adrenal insufficiency but higher than for hyperaldosteronism, adrenogenital disorders, and adrenomedullary hyperfunction. (health.mil)
  • Introduction: Autoimmune polyendocrine syndrome type I (APS-1) also called autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic autosomal recessive disease known by the triad of the major components hypoparathyroidism, primary adrenocortical insufficiency and chronic mucocutaneous candidosis. (eurospe.org)
  • Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. (nih.gov)
  • Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. (nih.gov)
  • A syndrome caused by high levels of cortisol in the blood either due to excessive production and secretion of corticosteroids secondary to pituitary or adrenocortical neoplasms, or intake of glucocorticoid drugs. (icd9data.com)
  • McCune-Albright syndrome (MAS) consists of at least two of the following three features: (1) polyostotic fibrous dysplasia (PFD), (2) café-au-lait skin pigmentation (see the image below), and (3) autonomous endocrine hyperfunction (eg, gonadotropin-independent precocious puberty ). (medscape.com)
  • OMIM#174800) is a rare disorder hallmarked by the triad fibrous osseous dysplasia, cafè-au-lait skin spots and endocrine hyperfunctions, usually peripheral precocious puberty. (eurospe.org)
  • Although the action of corticotropin is similar to that of exogenous adrenocortical steroids the quantity of adrenocorticoid may be variable. (nih.gov)
  • Adrenocortical hyperfunction is a condition where there is an overexpression of products of the adrenal cortex. (wikipedia.org)
  • Purified Cortrophin Gel is the anterior pituitary hormone which stimulates the functioning adrenal cortex to produce and secrete adrenocortical hormones. (nih.gov)
  • Hyperfunction of the adrenal cortex. (synthroidnews.net)
  • Kona syndrome (primary aldosteronism) develops in 1/3 cases of hyperfunction of the adrenal cortex. (synthroidnews.net)
  • Myxoid adrenocortical adenoma is a rare adenoma originated from adrenal cortex. (endocrine-abstracts.org)
  • Testicular or ovarian hyperfunction is the most common abnormality. (medscape.com)
  • Dexamethasone sodium phosphate, a synthetic adrenocortical steroid, is a white or slightly yellow, crystalline powder. (nih.gov)
  • In our experience, survival of patients with adrenocortical adenomas has been 100%, whereas only five of nine children with adrenocortical carcinomas survived, and four of the five were younger than 10 years of age. (nih.gov)