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Differential Diagnosis For Gait disturbance/abnormality: Hereditary, Familial, Genetic Disorders

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List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Oromandibular facial dystonia syndrome
Ataxia-telangiectasia
Cerebellar hereditofamilial degen.
Huntington's chorea
Neuropathy, sensory radicular, heredit.
Paraplegia, spastic hereditary
Peroneal muscular atrophy(Charcot Mar.)
Ataxia/Oculomotor apraxia syndrome (9p13.3)
Schilder disease/Adrenoleukodystrophy
Van Bogaert encephalitis
Dominant SCA/Spinal Cerebellar ataxias
Cerebellar ataxia, congenital/hered.
Cockayne syndrome
Dystonia musculorum deformans
Friedreich's Ataxia
Hallervorden-Spatz disease (PKAN/NBIA)
Hereditary/neurologic degeneration synd
Olivopontocerebellar degeneration
Osteodysplasia, familial (Melnick Needles)
Parkinsonism, juvenile, of Hunt
Pelizaeus-Merzbacher disease
Spinocerebellar ataxia, Hered/Type I
Torsion dystonia, primary/idiopathic
Cerebellar ataxia/Cayman type
Episodic ataxia/EA-2/Hemiplegic migraine
Hereditary sensory neuropathy (type II)
Segawa Syndrome/Infant Parkinsonism
Vitamin E deficiency/dependence familial ataxia
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