Autosomal dominant spastic paraplegia type 13

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Name:
Autosomal dominant spastic paraplegia type 13
Description:
A rare, pure or complex form of hereditary spastic paraplegia characterized by progressive spastic paraplegia with pyramidal signs in the upper and lower limbs, and decreased vibration sense.
ORPHAcode:
100994
Synonyms:
SPG13
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14