Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation

Disease Export to PDF
Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation
Description:
A rare autosomal dominant hereditary axonal motor and sensory neuropathy characterized by childhood onset of slowly progressive distal muscle weakness and atrophy primarily affecting the lower limbs, associated with sensory impairment and ataxia presenting with an unsteady, broad-based gait and frequent falls. Additional signs include decreased deep tendon reflexes and hand tremor.
ORPHAcode:
487814
Synonyms:
CMT2 due to DGAT2 mutation
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14