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Differential Diagnosis For Ataxia: Hereditary, Familial, Genetic Disorders

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List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Ataxia-telangiectasia
Cerebellar hereditofamilial degen.
Hereditary neuropathy
Huntington's chorea
Myoclonic encephalopathy/childhood
Neuropathy, hypertrophic interstitial
Neuropathy, sensory radicular, heredit.
Paraplegia, spastic hereditary
Peroneal muscular atrophy(Charcot Mar.)
Ataxia/Oculomotor apraxia syndrome (9p13.3)
Mitochondrial myopathy/MERRF
Schilder disease/Adrenoleukodystrophy
Dominant SCA/Spinal Cerebellar ataxias
Cerebellar ataxia, congenital/hered.
Cockayne syndrome
Dentatorubral-Pallidoluysian Atrophy (DRPLA)
Encephalomyelopathy/necro/subact/Leigh
Friedreich's Ataxia
Hallervorden-Spatz disease (PKAN/NBIA)
Hereditary mitochondrial disorder
Hereditary/neurologic degeneration synd
Kearns-Sayre Ophthalmoplegic Syndrome
Leukodystrophy, Krabbe
Olivopontocerebellar degeneration
Parkinsonism, juvenile, of Hunt
Pelizaeus-Merzbacher disease
Refsum's disease
Roussy-Levy syndrome
Spinocerebellar ataxia, Hered/Type I
Spinopontine Atrophy /MJD disease
Von Hipple-Lindau disease/Retinocerebellar angiomas
Episodic ataxia/EA-2/Hemiplegic migraine
Giant axonal neuropathy, hereditary
Hereditary dysmyelinating neuropathy
Hereditary sensory neuropathy (type II)
Neuhauser Syndrome
Rosenberg-Bergstrom Syndrome
Segawa Syndrome/Infant Parkinsonism
Vitamin E deficiency/dependence familial ataxia
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