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

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Gait disturbance/abnormality
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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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