Lower Limb Deformity Caused by Hereditary and Metabolic Diseases

Hereditary sensorimotor neuropathy (Charcot–Marie–Tooth, CMT) is a progressive, neuromuscular atrophy syndrome which is known clinically as fibula muscular atrophy or hereditary motor sensory neuropathy; it is the most common autosomal dominant genetic disorder in the peripheral nervous system, most of which occur in childhood and adolescence.