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Differential Diagnosis For Prader-Willi syndrome - Rule Outs, Family history/Gait disorders

List of current finding(s):

Prader-Willi syndrome - Rule Outs
Family history/Gait disorders
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Allergic, Collagen, Auto-Immune Disorders: Chorea, Sydenham's acute
Metabolic, Storage Disorders: Wilsons Disease
Hereditary, Familial, Genetic Disorders: Ataxia-telangiectasia; Cerebellar hereditofamilial degen.; Huntington's chorea; Peroneal muscular atrophy(Charcot Mar.); Ataxia/Oculomotor apraxia syndrome (9p13.3); Dominant SCA/Spinal Cerebellar ataxias; Cerebellar ataxia, congenital/hered.; Dentatorubral-Pallidoluysian Atrophy (DRPLA); Dystonia musculorum deformans; Friedreich's Ataxia; Hallervorden-Spatz disease (PKAN/NBIA); Laurence-Moon-Biedel syndrome; Pelizaeus-Merzbacher disease; Refsum's disease; Spinocerebellar ataxia, Hered/Type I; Torsion dystonia, primary/idiopathic
Usage, Degenerative, Necrosis, Age Related Disorders: Parkinson's disease (paralysis agitans)

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