Autosomal recessive spastic paraplegia type 24

Orpha code: 101004OMIM code: 607584

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.

Disease data
Classification

Disease

Synonyms
SPG24
SPG24
ORPHA code
101004
OMIM code
607584
ICD10 code
G11.4
ICD11 code
-

No additional description.

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