Autosomal dominant Charcot-Marie-Tooth disease type 2A1
What is Autosomal dominant Charcot-Marie-Tooth disease type 2A1?
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, presenting with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor.
Other condition names
- CMT2A1
Inheritance type
Autosomal dominant
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Childhood
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.