Abstract
Dejerine-Sottas syndrome (DSS) is a progressive hypertrophic interstitial neuropathy of childhood characterized by defects in the myelin structure, with motor nerve conduction velocities below 10 m/sec. The phenotype is genetically heterogeneous with autosomal dominant and autosomal recessive inheritance but “de novo” mutations are also described. Nerve pathology is highly variable. The clinical course is severe, leading to sensory loss, distal followed by proximal weakness, foot deformities, scoliosis and contractures, cranial nerve deficits and occasionally spinal cord compression. In this case study we evaluated a case of DSS at a ten year old boy and we outlined the importance of the electrophysiological investigations together with magnetic resonance neurography in diagnosing the Dejerine-Sottas syndrome.
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