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Differential Diagnosis For Family history/Gait disorders


List of current finding(s):

Allergic, Collagen, Auto-Immune Disorders
Chorea, Sydenham's acute
Metabolic, Storage Disorders
Wilsons Disease
Hereditary, Familial, Genetic Disorders
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)
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)
AMBULATION DIS NEUROLOGIC, Ambulation Disorder Neurologic, Ambulation Disorders Neurologic, Family history, GAIT DIS NEUROLOGIC, Gait Disorder Neurologic, Gait Disorders Neurologic, Gait Dysfunction Neurologic, Gait Dysfunctions Neurologic, LOCOMOTION DIS NEUROLOGIC, Locomotion Disorder Neurologic, Locomotion Disorders Neurologic, NEUROLOGIC AMBULATION DIS, Neurologic Ambulation Disorder, Neurologic Ambulation Disorders, Neurologic Gait Disorder, Neurologic Gait Disorders, Neurologic Gait Dysfunction, Neurologic Gait Dysfunctions, NEUROLOGIC LOCOMOTION DIS, Neurologic Locomotion Disorder, Neurologic Locomotion Disorders
External Links Related to Family history/Gait disorders
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)