Orphanet: Autosomal dominant spastic paraplegia type 36
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Autosomal dominant spastic paraplegia type 36

Disease definition

A complex form of hereditary spastic paraplegia, characterized by an onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait, spasticity, lower limb weakness, pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy.

ORPHA:320365

Classification level: Disorder
  • Synonym(s):
    • SPG36
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adolescent, Adult
  • ICD-10: G11.4
  • OMIM: 613096
  • UMLS: C2936879
  • MeSH: -
  • GARD: -
  • MedDRA: -

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