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Charcot-Marie-Tooth disease type 2B
rareAutosomal dominant Charcot-Marie-Tooth disease type 2B (CMT2B) is a severe form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2B onset, in the 2nd or 3rd decade, is characterized by ulcerations and infections of feet. Symmetric and distal weakness develops mostly in the legs together with a severe symmetric distal sensory loss, tendon reflexes are only reduced at ankles and foot deformities, including pes cavus or planus and hammer toes, appear in childhood.
- Identifiers
- MONDO:0010949 OMIM:600882Orphanet:99936
- Causal genes
- RAB7A
- Also known as
- autosomal dominant Charcot-Marie-Tooth disease type 2B · Charcot Marie Tooth disease type 2B · Charcot-Marie-Tooth disease type 2 caused by mutation in RAB7A · Charcot-Marie-Tooth disease, axonal, type 2B · Charcot-Marie-Tooth disease, neuronal, type 2B
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