Syndrome acquired or congenital. Medical search. Frequent questions

Call 310-825-9011 to learn more about adult congenital heart disease treatment. (uclahealth.org)
The Ahmanson/UCLA Adult Congenital Heart Disease Center is the first and one of the largest facilities of its kind in the United States. (uclahealth.org)
The program is the combined efforts of the Division of Pediatric Cardiology and the Ahmanson/UCLA Adult Congenital Heart Disease Center. (uclahealth.org)
Patients who are new to the Ahmanson/UCLA Adult Congenital Heart Disease Center should ideally have their doctor's mail or fax in cardiac related medical records prior to scheduling an appointment. (uclahealth.org)

The program provides comprehensive treatment of adolescents with congenital heart disease, ages 15 to 20. (uclahealth.org)

What is nephrotic syndrome? (childrenshospital.org)
Nephrotic syndrome (NS) is the name given to a collection of kidney-related findings in your child's body. (childrenshospital.org)
While nephrotic syndrome is not a disease , it can be the first sign of disease that can damage the kidney's tiny blood-filtering unit (glomeruli) where urine is made. (childrenshospital.org)
Nephrotic syndrome always affects both kidneys. (childrenshospital.org)
There are thought to be two forms of nephrotic syndrome, minimal change disease (MCD) and focal sclerosis (FSGS). (childrenshospital.org)
What's the long-term outlook for a child with nephrotic syndrome? (childrenshospital.org)
Why is nephrotic syndrome a concern? (childrenshospital.org)
What are the different types of nephrotic syndrome? (childrenshospital.org)
One way to categorize types of nephrotic syndrome is by what's causing them. (childrenshospital.org)
Idiopathic nephrotic syndrome-the kind most children have-occurs for a reason that is unknown. (childrenshospital.org)
It's another way to look at nephrotic syndrome is in terms of how the affected tissue appears under a microscope, since this often correlates with treatment and outcome. (childrenshospital.org)
While "congenital" means present at birth, congenital nephrotic syndrome is usually discovered when a baby is a few months old, although it may take up to a year. (childrenshospital.org)

This statement summarizes the goals and current strategies for measles, rubella, and congenital rubella syndrome (CRS) elimination and for mumps reduction in the United States. (cdc.gov)
U.S. Public Health Service year 2000 objectives include eliminating measles, rubella, and congenital rubella syndrome, and reducing mumps incidence to less than 500 reported cases per year. (cdc.gov)
Congenital rubella syndrome (CRS) cases will be classified epidemiologically as internationally imported or U.S.-acquired, according to the source of infection in the mother, using the definitions below, which parallel the classifications for rubella cases. (cdc.gov)

Including human immunodeficiency virus (HIV) infection that leads to acquired immunodeficiency syndrome (AIDS), they have been recognized as a major public health problem for many years. (who.int)

Respiratory insufficiency and hypoventilation syndromes 32. (muni.cz)
Background: Central alveolar hypoventilation syndromes (CHS) encompass neurorespiratory diseases resulting from congenital or acquired neurological disorders. (eurekaselect.com)
Acquired central hypoventilation syndrome (e.g. (sp-ps.de)

The duration of vaginoplasty operations in cases of congenital vaginal tightness, absence or shortness of vagina is longer. (eserdag.com)
We compared maternal sociodemographic characteristics and health care utilization related to cases of congenital syphilis during the periods from 2001 to 2006 and from 2007 to 2011. (scielo.br)

Any congenital or acquired disturbances of the HPG axis could lead to the clinical syndrome of hypogonadism. (frontiersin.org)
Primary and secondary hypogonadism can be subdivided further by congenital and acquired etiologies ( Table 1 ). (aafp.org)
Primary hypogonadism (congenital or acquired): testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, or orchidectomy. (sideload.com)
Klinefelter Syndrome Klinefelter syndrome is a relatively common chromosomal abnormality characterized by hypogonadism, azoospermia, and elevated gonadotropin levels in association with a 47,XXY karyotype. (health.am)

Brown's atavistic superior oblique syndrome: etiology of different types of motility disorders in congenital Brown's syndrome]. (nih.gov)
Immune deficiency disorders are classified as either primary (congenital) or acquired. (ssa.gov)
PDR) The AHFS gives the same contraindications, but adds a history of Guillaine-Barre syndrome and = bleeding disorders which would contraindicate intramuscular injection. (faqs.org)
Congenital disorders may be inherited as autosomal dominant disorders or autosomal recessive disorders or have other causes (eg, sporadic mutations, chromosomal abnormalities, teratogens). (msdmanuals.com)
Congenital complement disorders may also increase the risk of hemolytic-uremic sydrome (HUS) following infection. (merckmanuals.com)
Bone marrow failure syndrome (BMFS) is a group of disorders that may manifest as single cytopenia (eg, erythroid, myeloid, or megakaryocytic) or as pancytopenia. (medscape.com)

Alders M, Bikker H, Christiaans I. Long QT Syndrome. (medlineplus.gov)
Congenital and acquired long QT syndrome. (medlineplus.gov)
Long QT syndrome (LQTS) is a congenital disorder characterized by a prolongation of the QT interval on electrocardiograms (ECGs) and a propensity to ventricular tachyarrhythmias, which may lead to syncope, cardiac arrest, or sudden death. (medscape.com)
Marked prolongation of QT interval in a 15-year-old male adolescent with long QT syndrome (LQTS) (R-R = 1.00 s, QT interval = 0.56 s, QT interval corrected for heart rate [QTc] = 0.56 s). (medscape.com)
Long QT syndrome is a condition that affects the electrical system of the heart . (kidshealth.org)
What Happens in Long QT Syndrome? (kidshealth.org)
What Are the Signs & Symptoms of Long QT Syndrome? (kidshealth.org)
Some kids with long QT syndrome have no symptoms. (kidshealth.org)
Congenital long QT syndrome can be treated, but it can't be "cured" and won't go away on its own. (kidshealth.org)
Acquired long QT syndrome usually stops if the cause (like certain medicines) goes away. (kidshealth.org)
Long QT syndrome can affect people of all ages, but is sometimes more serious in children. (kidshealth.org)
How Is Long QT Syndrome Diagnosed? (kidshealth.org)
To diagnose long QT syndrome, doctors will ask about a child's health history and the family's health history. (kidshealth.org)
How Is Long QT Syndrome Treated? (kidshealth.org)
Often doctors can treat long QT syndrome with medicines called beta blockers. (kidshealth.org)
For children who have congenital long QT syndrome, treatment usually won't make the QT interval shorter. (kidshealth.org)
By following the cardiologist's advice about medicines, diet, and exercise, most kids with long QT syndrome can stay healthy. (kidshealth.org)
The family history of cardiovascular diseases is considered positive in athletes when close relatives had experienced a premature heart attack or sudden death (below 55 years of age in males and 65 years in females), or suffered from cardiomyopathy, Marfan syndrome, long QT syndrome, Brugada syndrome, severe arrhythmias, coronary artery disease, or other disabling cardiovascular diseases. (escardio.org)

The majority of instances of heterochromia are hereditary and these might be associated with a congenital syndrome. (disabled-world.com)
Hereditary marrow failure syndromes. (medscape.com)

These abnormalities can arise from traumatic brain injuries, strokes and other vascular problems, infections of the nervous system (meningitis or encephalitis), congenital malformations, brain tumors or metabolic abnormalities. (hopkinsmedicine.org)
Skeletal abnormalities, such as short stature and scoliosis are seen in the LQT7 type (Andersen syndrome), and congenital heart diseases, cognitive and behavioral problems, musculoskeletal diseases, and immune dysfunction may be seen in those with LQT8 type (Timothy syndrome). (medscape.com)
However, other cardiovascular abnormalities such as anomalies of coronary vessels, arrhythmogenic dysplasia of right ventricle (ADRV), mitral valve prolapse, myocarditis, coronary vessel bridge, Marfan Syndrome, bicuspid aortic valve, pulmonary thrombo-embolism and channelopathies also significantly contribute to cardiovascular risk in athletes. (escardio.org)
The etiology of bone marrow failure (BMF) includes defective stem/progenitor cells and/or stroma/accessory cells/growth factors, as well as deficient nonspecific nutrients or, as in the case of acquired aplastic anemia, immune-mediated abnormalities. (medscape.com)

According to the various accessible medical records, hypertrophic cardiomyopathy (HCM), congenital heart defects, premature coronary artery disease are the most frequent causes of cardiovascular events in athletes (2,3). (escardio.org)

Congenital heart diseases in adults 19. (muni.cz)
Distinguished pediatric surgeon Samuel M. Alaish, M.D., will join the Johns Hopkins Children's Center to co-lead its newly formed Center for Intestinal Rehab and Cure Using Science (CIRCUS), a multidisciplinary program dedicated to the study and care of children with short bowel syndrome, a condition marked by insufficient gut tissue or poor gut function due to acquired or congenital diseases. (hopkinsmedicine.org)

Mibavademab is under clinical development by Regeneron Pharmaceuticals and currently in Phase II for Acquired Generalized Lipodystrophy (Lawrence Syndrome). (pharmaceutical-technology.com)
According to GlobalData, Phase II drugs for Acquired Generalized Lipodystrophy (Lawrence Syndrome) does not have sufficient historical data to build an indication benchmark PTSR for Phase II. (pharmaceutical-technology.com)
Mibavademab is under development for the treatment of congenital or acquired generalized lipodystrophy and obesity. (pharmaceutical-technology.com)

Toremifene should not be prescribed to patients with congenital/acquired QT prolongation, uncorrected hypokalemia, or uncorrected hypomagnesemia. (drugs.com)

In probable cases, either or both of the eye-related findings (cataracts and congenital glaucoma) count as a single complication. (cdc.gov)

Acute coronary syndrome 27. (muni.cz)
Hemolytic-uremic syndrome (HUS) is an acute, fulminant disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and acute kidney injury. (merckmanuals.com)
Infection by Escherichia coli O157:H7 and Other Enterohemorrhagic E. coli (EHEC) The gram-negative bacteria Escherichia coli O157:H7 and other enterohemorrhagic E. coli (EHEC) typically cause acute bloody diarrhea, which may lead to hemolytic-uremic syndrome. (merckmanuals.com)

Pulmonary arteriovenous malformations may also be acquired rarely secondary to chronic infections such as schistosomiasis, actinomycosis, tuberculosis, and metastatic thyroid cancer. (medscape.com)

[ 3 ] Pulmonary arteriovenous malformations may also be an acquired condition found in patients with liver disease, mainly liver cirrhosis. (medscape.com)
Patients with congenital heart disease in whom the systemic venous return to the lungs does not include blood return from the hepatic veins also develop pulmonary arteriovenous malformations. (medscape.com)
The center is a tertiary care national and international resource that provides services to the growing number of patients with congenital heart disease who reach adulthood. (uclahealth.org)
Findings on physical examination usually do not indicate a diagnosis of LQTS, although some patients may present with excessive bradycardia for their age, and some patients may have hearing loss (congenital deafness), indicating the possibility of Jervell and Lange-Nielsen syndrome. (medscape.com)
Dr. Boada provides clinical neuropsychological services for patients, and training and supervision for postdoctoral residents, through the outpatient Epilepsy and Acquired Brain Injury Clinic. (kennedykrieger.org)
Four of 22 consecutive patients (18%) treated at Indiana University for primary mediastinal germ cell tumors had karyotypic confirmation of Klinefelter syndrome, and an additional patient had clinical features. (health.am)
The average age of patients with Klinefelter syndrome who develop extragonadal germ cell tumors is approximately 18 years, 10 years younger than the median age of those developing this tumor in the absence of Klinefelter syndrome. (health.am)
In patients with Sturge-Weber syndrome, X-ray findings in the skull usually show a tram-track pattern of calcification that is caused by calcification in opposing gyri on either side of an intervening dilated sulcus. (medscape.com)
All patients critical for the comprehensive and optimum were finally diagnosed in the main referral care of congenital heart disease population institutes. (who.int)
A significant number of referrals (234 are also considered of pivotal importance of 974, i.e. around 24% in the Al Hasaa for groups which care for patients with study) were normal and excluded from the congenital heart disease as well as for poli- study. (who.int)
Patients with acquired heart disease cymakers. (who.int)

Mutations in these genes are causes of congenital hypopituitarism and have specific pituitary hormone deficiencies associated with the involved gene. (medscape.com)
Complement dysregulation is usually from a mutation in genes controlling complement proteins or factors but sometimes from acquired autoantibodies to certain complement factors. (merckmanuals.com)
all genes associated with this syndrome (ie, DKC1 , TERT, TERC, NOP10 ) encode proteins in the telomerase complex responsible for maintaining telomeres at the ends of chromosomes. (medscape.com)

Sturge-Weber Syndrome: Sturge-Weber syndrome is characterized by a port-wine stain in the distribution of the trigeminal nerve on the person's face and tumors known as, 'angiomas,' of their choroid and brain. (disabled-world.com)
Sturge-Weber syndrome is sporadic neurocutaneous syndrome. (medscape.com)
Cite this: Sturge-Weber Syndrome - Medscape - Jan 01, 2008. (medscape.com)

Congenital heterochromia might be familial and is inherited as an autosomal dominant trait. (disabled-world.com)

Alaish's interest in short bowel syndrome was sparked by his clinical encounters in the neonatal intensive care unit during his fellowship. (hopkinsmedicine.org)
She provides clinical neuropsychological services through the Department of Neuropsychology's outpatient specialty clinics, including the Congenital/Genetic Conditions Clinic and the Assessment Services in neuroPsychology for Initial and Return Evaluations (ASPIRE) Clinic, which she currently coordinates. (kennedykrieger.org)
alternatively, congenital syphilis might present as a syndrome with various clinical manifestations such as massive sepsis, bone lesions, and cutaneous-mucous and central nervous system lesions. (scielo.br)

Dr. Caldwell is also a primary supervisor for the Congenital/Genetic Conditions Outpatient Major Rotation. (kennedykrieger.org)

The association of Klinefelter syndrome and mediastinal nonseminomatous germ cell tumors is now well recognized. (health.am)

Piebaldism': Piebaldism is similar to Waardenburg syndrome, although it is not associated with deafness. (disabled-world.com)

Ventricular septal defects (VSDs) are congenital or acquired defects in the interventricular septum that allow shunting of blood between the left and right ventricles. (bmj.com)

To be classified as an internationally imported CRS case, the mother must have acquired rubella infection outside the U.S. or in the absence of documented rubella infection, the mother was outside the United States during the period when she may have had exposure to rubella that affected her pregnancy (from 21 days before conception and through the first 24 weeks of pregnancy). (cdc.gov)
At the conclusion of today's session, the participant will be able to: understand the latest estimates for birth defects associated with Zika virus infection during pregnancy,discuss additional considerations for evaluating and managing infants with possible congenital Zika virus infection, and apply the updated recommendations outlined in the additional considerations for the evaluation and management of infants with possible congenital Zika virus infection. (cdc.gov)

24.9%) had neonatal congenital heart disease. (who.int)

We are pleased to announce the creation of the Adolescent/Young Adult Transitional Care Program, for Congenital Heart Disease . (uclahealth.org)
ABSTRACT To provide an overview of the epidemiology of congenital heart disease, the results of epidemiological studies done in 4 regions of Saudi Arabia (August 1988-February 2000) and 2604 individuals with congenital heart disease were evaluated. (who.int)
Knowledge of the epidemiology authors of these studies (qualified paediatric of congenital heart disease is the basis on cardiologists) aided by qualified paediatric which investigative efforts will emerge to specialists made the diagnostic decisions identify the causes of cardiac dysmorpho- after carrying out a full physical examina- genesis and afford opportunities to prevent tion, plain chest radiography, electrocardi- them [ 3 ]. (who.int)

Torsade de pointes, often referred to as torsade, is associated with a prolonged QT interval, which may be congenital or acquired. (medscape.com)

During the reconstruction of a heart with hypoplastic left heart syndrome, the surgical team alters the heart and circulatory system. (chop.edu)

Other instances are acquired and caused by an injury or disease. (disabled-world.com)
Cystic kidney disease may be congenital or acquired. (msdmanuals.com)

A condition with congenital and acquired forms causing recurrent ulcers in the fingers and toes. (harvard.edu)

Superior oblique tendon trochlear passage syndrome : Causes, motility findings and treatment of acquired Jaensch-Brown syndrome]. (nih.gov)
Horner's Syndrome: Horner's syndrome is not a form of genetic syndrome, but a group of findings due to intrauterine brain injury or birth injury involving the person's sympathetic nervous system innervation to one eye. (disabled-world.com)

GLUT-1 deficiency syndrome is an example of an epilepsy caused by a metabolic problem. (hopkinsmedicine.org)

Usually congenital, but rarely acquired after myocardial infarction or trauma. (bmj.com)

However, during his rounds Alaish noticed that bile backup was also rather common among babies with short bowel syndrome and among premature babies who require intravenous nutrition known as TPN. (hopkinsmedicine.org)

A cardiologist at the local hospital told Julia and her husband, Jeremy, that their baby likely had hypoplastic left heart syndrome (HLHS) , a single ventricle heart defect . (chop.edu)
In this complex congenital heart defect, the heart is unable to pump properly because its left side is underdeveloped. (chop.edu)
Hypoplastic left heart syndrome (HLHS) is a severe congenital heart defect in which the left side of the heart is underdeveloped. (chop.edu)
These data suggest that either a congenital or an acquired germ cell defect contributes not only to defective spermatogenesis but also to the development of extragonadal germ cell tumors. (health.am)

The high incidence of congenital syphilis in Mato Grosso and the low levels of health care indicators for pregnant women with syphilis suggest the need to improve the coverage and quality of prenatal care. (scielo.br)

A descriptive study cross-sectional and of time trends assessing the congenital syphilis was performed in Cuiabá and Mato Grosso between 2001 and 2011. (scielo.br)

Bone marrow section from a 7-year-old girl with idiopathic acquired aplastic anemia. (medscape.com)

Inherited bone marrow failure syndrome (genetics known and presumed). (medscape.com)

Data have been used to estimate the number of fetuses and infants with birth defects potentially related to Zika, provide information on the phenotype of congenital Zika syndrome, and plan for services for pregnant women, their infants, and families affected by Zika to ensure infants are linked to care. (cdc.gov)

Significant left-to-right shunting results in pulmonary hypertension, which, if left untreated, can progress to shunt reversal with cyanosis and Eisenmenger syndrome. (bmj.com)

The Fontan circulation drastically increases survival rates for children with hypoplastic left heart syndrome. (chop.edu)
When Lily was 3½ she had her third operation for hypoplastic left heart syndrome, known as the Fontan operation. (chop.edu)

Horner's syndrome is not associated with hearing loss or additional pigmentation anomalies. (disabled-world.com)

These changes can be present at birth (congenital) or acquired later in life. (hopkinsmedicine.org)
Heterochromia is classified mainly by its time of onset as either genetic or congenital, present at or shortly after birth, or acquired. (disabled-world.com)
Congenital vagina stenosis includes situations about vaginal narrowness which comes since from the birth. (eserdag.com)

Congenital syndromes which might be characterized by heterochromia iridis include the following. (disabled-world.com)

Anatomy4

Organisms3

Diseases194

Chemicals and Drugs6

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Psychiatry and Psychology8

Phenomena and Processes23

Information Science6

Named Groups1

Health Care16

Adult congenital heart d4

Adolescents with congenital heart d1

Nephrotic12

Rubella syndrome3

Immunodeficiency syndrome1

Hypoventilation3

Cases of congenital2

Hypogonadism4

Disorders6

Long QT syndr18

Hereditary2

Abnormalities4

Hypertrophic Cardiomyopathy1

Diseases2

Lipodystrophy3

Prolongation1

Glaucoma1

Acute3

Chronic1

Patients11

Genes3

Sturge-Weber Sy3

Autosomal1

Clinical3

Primary1

Klinefelter1

Deafness1

Ventricular1

Infection2

Neonatal1

Heart disease3

Prolonged QT inter1

Surgical1

Disease2

Recurrent1

Findings2

Metabolic1

Rarely1

Premature1

Defect4

Incidence1

20011

Idiopathic1

Genetics1

Infants1

Pulmonary1

Hypoplastic2

Anomalies1

Birth3

Include1