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Charcot-Marie-Tooth disease type 2B

rare

Autosomal 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.

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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