Orphanet: Autosomal recessive spastic paraplegia type 24
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Autosomal recessive spastic paraplegia type 24

Disease definition

A very rare, pure form of spastic paraplegia characterized by an onset in infancy of lower limb spasticity associated with gait disturbances, scissor gait, tiptoe walking, clonus and increased deep tendon reflexes. Mild upper limb involvement may occasionally also be associated.

ORPHA:101004

Classification level: Disorder
  • Synonym(s):
    • SPG24
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy
  • ICD-10: G11.4
  • OMIM: 607584
  • UMLS: C1843569
  • MeSH: -
  • GARD: 9296
  • MedDRA: -

  A summary on this disease is available in Français (2019) Deutsch (2019) Español (2019) Italiano (2019) Nederlands (2019)

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FSMR : produced/endorsed by FSMR(s)

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