DiseasesChemicals and DrugsAnalytical, Diagnostic and Therapeutic Techniques and EquipmentPsychiatry and PsychologyDisciplines and OccupationsAnthropology, Education, Sociology and Social PhenomenaHumanitiesInformation ScienceNamed Groups
Shy-Drager SyndromeVentilators, MechanicalSyndromeShynessMultiple System AtrophyPhysical and Rehabilitation MedicineEncyclopedias as TopicSpeech TherapyOccupational TherapySpeech DisordersHomeopathyArchivesParentsDyslexiaMateria MedicaMuscular Dystrophies
Olivopontocerebellar atrophyStriatonigralParkinsonianSporadicIdiopathicParkinson'sAtaxiaAlpha-synucleinInclusion bodiesDiagnosisCongenitalDiseaseCharacteristicGeneticDistinctSymptomsSeverePatientsNormalResultWhiteStudyStriatonigral degenerationNeuromuscularAutonomicParkinson's DiseaseInclusionOrthostaticChronicClinicalIncludeDeathTermAidsMultipleCaseBlood
Olivopontocerebellar atrophy4
Striatonigral1
  • While symptoms of autonomic failure and cerebellar degeneration may be present in striatonigral degeneration, the predominant finding is parkinsonism. (medscape.com)
Parkinsonian5
  • Many neurologists find this a useful term for the autonomic presentation, but consideration must be given to whether subtle parkinsonian or cerebellar findings are present, in which case the MSA-P or MSA-C classifications, respectively, would be more appropriate. (medscape.com)
  • However, because of the common parkinsonian features, the disorders have been collectively named Parkinson-plus syndromes. (medscape.com)
  • An inadequate response to treatment in a patient with parkinsonian symptoms suggests the possibility of a Parkinson-plus syndrome and warrants a search for the signs and symptoms of degeneration in other neuronal systems. (medscape.com)
  • There is no ideal way to define and distinguish Parkinson's disease from other parkinsonian syndromes. (parkinson.ca)
  • Parkinson disease is by far the most common cause of the parkinsonian syndrome , accounting for approximately 80% of cases (the remainder being due to other neurodegenerative diseases, such as Lewy body dementia ) 1 . (radiopaedia.org)
Sporadic2
  • Other manifestations of multiple system atrophy are Shy-Drager syndrome, in which autonomic failure predominates, and sporadic olivopontocerebellar degeneration, which is characterized primarily by cerebellar signs. (medscape.com)
  • After four or five years of increasing dosages their effect becomes sporadic and unpredictable (the "on-off syndrome") and patients become increasingly helpless and depressed. (digitalnaturopath.com)
Idiopathic1
Parkinson's1
  • The most common first sign of MSA is the appearance of an "akinetic-rigid syndrome" (i.e. slowness of initiation of movement resembling Parkinson's disease) found in 62% at first presentation. (wikipedia.org)
Ataxia3
  • The group of disorders classified under multiple system atrophy belong to a broader class called the Parkinson-plus syndromes , which have in common features such as bradykinesia and rigidity seen in Parkinson disease, combined with additional components such as autonomic dysfunction, ataxia, or dementia. (medscape.com)
  • Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective. (nih.gov)
  • Conventional brain MRI findings of patients with neuronal intranuclear hyaline inclusion disease strongly resemble those seen in fragile X-associated tremor/ataxia syndrome (FXTAS) , including symmetric white matter involvement in combination with hyperintense changes of the middle cerebellar peduncles 4 . (radiopaedia.org)
Alpha-synuclein3
  • The purpose of revisiting this topic was to incorporate advances in research, such as the identification of alpha-synuclein as a key pathologic finding, and to simplify the original diagnostic criteria. (medscape.com)
  • The presence of cortical Lewy bodies is confirmed by the finding of alpha synuclein positive rounded cytoplasmic inclusion in neurons. (medscape.com)
  • A characteristic finding is cytoplasmic inclusion bodies containing alpha-synuclein within oligodendroglial cells. (msdmanuals.com)
Inclusion bodies1
  • [ 3 ] The identification of these inclusion bodies was a unifying factor in the pathologic classification of the 3 entities that now fall under the category of multiple system atrophy: MSA-P, MSA-C, and, less formally, Shy-Drager syndrome. (medscape.com)
Diagnosis1
  • Congenital central hypoventilation syndrome: diagnosis and management. (nih.gov)
Congenital1
  • Development of a peripheral популярные vision for cirrhosis in files finding with HIV in chromosomal spaces: congenital health members Evaluation of autoimmune contractions. (reconcile-int.org)
Disease6
  • Parkinson-plus syndromes respond poorly to the standard treatments for Parkinson disease (PD). (medscape.com)
  • High-risk patients with cardiovascular or structural heart disease, history concerning for arrhythmia, abnormal electrocardiographic findings, or severe comorbidities should be admitted to the hospital for further evaluation. (aafp.org)
  • Patients with syncope and evidence of congestive heart failure or structural heart disease, abnormal electrocardiographic findings, or a family history of sudden death should be admitted to the hospital for emergent evaluation. (aafp.org)
  • Patients with syncope who are at low risk of adverse events (e.g., those with symptoms consistent with vasovagal or orthostatic hypotension syncope, no history of heart disease, no family history of sudden cardiac death, and normal electrocardiographic findings) may be safely followed without further intervention or treatment. (aafp.org)
  • AIDS-like syndrome: AIDS-like disease (illness) (syndrome) ARC AIDS-related complex Pre-AIDS AIDS-related conditions Prodromal-AIDS 3. (cdc.gov)
  • They conclude that these findings suggest some of the typical brain abnormalities seen in Alzheimer's disease "can be induced by a prion-like mechanism of disease transmission through propagation of protein misfolding. (alzheimerdisease.tv)
Characteristic1
  • [5] [6] By the late 1800s, an exhaustive body of literature had been produced on the gross anatomical findings characteristic of known diseases. (bionity.com)
Genetic2
  • Modern immunocytochemical techniques and genetic findings suggest that Parkinson-plus syndromes can be broadly grouped into 2 types: synucleinopathies and tauopathies. (medscape.com)
  • In this tuberculosis we will be the curable conditions for working genetic pigs into a Web syndrome, petting at strongly the Pseudomembranous JSF 2 concepts and the review located by CDI. (reconcile-int.org)
Distinct1
Symptoms1
  • His magnum opus, De Sedibus et Causis Morborum per Anatomem Indagatis , published in 1761, describes the findings of over 600 partial and complete autopsies, organised anatomically and methodically correlated with the symptoms exhibited by the patients prior to their demise. (bionity.com)
Severe2
  • MSA is also different from multiple organ dysfunction syndrome, sometimes referred to as multiple organ failure, and from multiple organ system failures, an often-fatal complication of septic shock and other severe illnesses or injuries. (wikipedia.org)
  • This is also considered as severe treatment, or safety in the syndrome. (reconcile-int.org)
Patients1
  • A follow-up study was unable to replicate this finding in American MSA patients. (wikipedia.org)
Normal1
  • Thus, pure small fiber neuropathies may be associated with normal findings on routine electrophysiologic studies. (medscape.com)
Result1
  • The bold DizzinessOne of condition Result for boards with HIV layer and latent trois syndrome is also declined. (reconcile-int.org)
White1
  • Bigger programs of the популярные комнатные растения распространенные виды сорта и in mouth may diagnose white to RIA bacteria that are syndrome of the rifampicin. (reconcile-int.org)
Study1
  • Their study findings also show that the drugs are not associated with increased mortality, as had been reported in an earlier study. (digitalnaturopath.com)
Striatonigral degeneration3
  • While symptoms of autonomic failure and cerebellar degeneration may be present in striatonigral degeneration, the predominant finding is parkinsonism. (medscape.com)
  • It includes 3 disorders previously thought to be distinct: olivopontocerebellar atrophy, striatonigral degeneration, and Shy-Drager syndrome. (msdmanuals.com)
  • MSA was formerly known as Shy-Drager syndrome, olivopontocerebellar atrophy (OCPA), or striatonigral degeneration. (nih.gov)
Neuromuscular1
  • Besides nerve localization in the peripheral nervous system, it occurs in diseases of the presynaptic neuromuscular junction such as botulism and myasthenic syndrome. (medscape.com)
Autonomic3
  • Other manifestations of multiple system atrophy are Shy-Drager syndrome, in which autonomic failure predominates, and sporadic olivopontocerebellar degeneration, which is characterized primarily by cerebellar signs. (medscape.com)
  • The group of disorders classified under multiple system atrophy belong to a broader class called the Parkinson-plus syndromes , which have in common features such as bradykinesia and rigidity seen in Parkinson disease, combined with additional components such as autonomic dysfunction, ataxia, or dementia. (medscape.com)
  • Many neurologists find this a useful term for the autonomic presentation, but consideration must be given to whether subtle parkinsonian or cerebellar findings are present, in which case the MSA-P or MSA-C classifications, respectively, would be more appropriate. (medscape.com)
Parkinson's Disease2
  • However, 'pill-rolling' Parkinson's disease tremor is often not exhibited in these other syndromes. (pharmacology2000.com)
  • The most common first sign of MSA is the appearance of an "akinetic-rigid syndrome" (i.e. slowness of initiation of movement resembling Parkinson's disease) found in 62% at first presentation. (wikipedia.org)
Inclusion1
  • [ 3 ] The identification of these inclusion bodies was a unifying factor in the pathologic classification of the 3 entities that now fall under the category of multiple system atrophy: MSA-P, MSA-C, and, less formally, Shy-Drager syndrome. (medscape.com)
Orthostatic1
  • Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. (bvsalud.org)
Chronic1
  • Chronic jupiter shitload resistance in which fortunate values of he man-made infection esophagus fat, difficult population site( MSA) is three organs usually Shy-Drager death, s une, and unconjugated leg. (reconcile-int.org)
Clinical3
  • Sleep-related breathing disorders are a group of clinical conditions ranging from habitual snoring to obstructive sleep apnea syndrome (OSAS) during the lifespan. (intechopen.com)
  • These findings served as the basis for a full-scale randomized clinical trial of cyclosporine as a method of treatment of Behcet's patients. (nih.gov)
  • Which of the following clinical findings is most likely? (thepalife.com)
Include1
  • This will include our assessment, any diagnostic findings, and plan of care. (vumc.org)
Death1
Term2
Aids2
  • 1. AIDS: Acquired immune deficiency syndrome Acquired immunodeficiency syndrome 2. (cdc.gov)
  • AIDS-like syndrome: AIDS-like disease (illness) (syndrome) ARC AIDS-related complex Pre-AIDS AIDS-related conditions Prodromal-AIDS 3. (cdc.gov)
Multiple1
  • MSA is also different from multiple organ dysfunction syndrome, sometimes referred to as multiple organ failure, and from multiple organ system failures, an often-fatal complication of septic shock and other severe illnesses or injuries. (wikipedia.org)
Case1
  • PMID- 5097502 TI - A pericentric inversion, 5 p-q+, and additional complex rearrangements in a case of cri-du-chat syndrome. (nih.gov)
Blood1