Autosomal recessive spastic paraplegia type 56

Disease Export to PDF
Name:
Autosomal recessive spastic paraplegia type 56
Description:
A rare form of hereditary spastic paraplegia characterized by delayed walking, toe walking, unsteady and spastic gait, hyperreflexia of the lower limbs, and extensor plantar responses. Upper limbs spasticity and dystonia, subclinical axonal neuropathy, cognitive impairment and intellectual disability have also been associated.
ORPHAcode:
320411
Synonyms:
SPG56
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14