ORPHA:101077
X-linked Charcot-Marie-Tooth disease type 3
Also called CMT3X, CMTX3
- Body system
- Neurological diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Adolescent, Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:101077 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Gait disturbance
- Motor delay
- Areflexia
- Abnormal foot morphology
- Pes cavus
- Decreased motor nerve conduction velocity