Autosomal recessive spastic paraplegia type 24

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Name:
Autosomal recessive spastic paraplegia type 24
Description:
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.
ORPHAcode:
101004
Synonyms:
SPG24
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14