Autosomal dominant Charcot-Marie-Tooth disease type 2DD

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2DD
Description:
A rare autosomal dominant hereditary axonal motor and sensory neuropathy characterized by predominantly distal weakness and muscle atrophy, decreased or absent tendon reflexes, and reduced vibratory sensation in the lower and upper extremities. Pes cavus develops in many patients. Additional symptoms like ataxia, tremor, or swallowing difficulties have been reported. Patients usually remain ambulatory even late in the disease. Age of onset ranges from childhood to adulthood, with earlier onset tending to be associated with a more severe disease phenotype.
ORPHAcode:
521414
Synonyms:
ATP1A1-related CMT2
ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
CMT2DD
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14