ORPHA:101075
X-linked Charcot-Marie-Tooth disease type 1
Also called CMT1X, CMTX1
- Body system
- Neurological diseases
- Inheritance pattern
- X-linked dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:101075 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Pes cavus
- Distal upper limb amyotrophy
- Distal lower limb amyotrophy
- Abnormal nerve conduction velocity
- Sensory neuropathy
- Areflexia