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MSA was first described in 1960 by Milton Shy and Glen Drager and was then known as Shy–Drager syndrome. [ 2 ] Many people affected by MSA experience dysfunction of the autonomic nervous system , which commonly manifests as orthostatic hypotension , impotence , loss of sweating , dry mouth and urinary retention and incontinence .
Multiple system atrophy (Shy–Drager syndrome) [6] Neuroacanthocytosis [6] Neuronal ceroid lipofuscinosis [6] Olivopontocerebellar atrophy [6] Pantothenate kinase-associated neurodegeneration, also known as neurodegeneration with brain iron accumulation [6] Parkin mutation causing hereditary juvenile dystonia [6] Parkinson's disease [6]
Parkinson-plus syndromes (PPS) are a group of neurodegenerative [1] diseases featuring the classical features of Parkinson's disease (tremor, rigidity, akinesia/bradykinesia, and postural instability) with additional features that distinguish them from simple idiopathic Parkinson's disease (PD).
Hereditary breast–ovarian cancer syndrome; Hereditary hyperbilirubinemia; ... Shwachman–Diamond syndrome; Shy-Drager syndrome; Sick building syndrome;
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Hereditary motor and sensory neuropathy with proximal dominance; I. ... Shy-Drager syndrome; Spinocerebellar ataxia; Subacute combined degeneration of spinal cord;
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
Shwachman–Bodian–Diamond syndrome; Shwartzman phenomenon; Shy–Drager syndrome; Si ... Sotos syndrome; Southwestern Athabaskan genetic diseases; Sp. Spa; Spe–Sph;