Autosomal recessive spastic paraplegia type 9B

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Name:
Autosomal recessive spastic paraplegia type 9B
Description:
A rare complex hereditary spastic paraplegia characterized by early onset of slowly progressive spastic para- or tetraparesis, increased tendon reflexes, positive Babinski sign, global developmental delay, cognitive impairment, and pseudobulbar palsy. Additional manifestations include dysmorphic facial features, tremor, short stature, and urinary incontinence.
ORPHAcode:
447760
Synonyms:
AR-SPG9B
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14