Back
Publications

Articles tagged with Dejerine-Sottas syndrome (DSS)

  • Dejerine-Sottas Syndrome Panel

    Dejerine-Sottas syndrome (DSS) is a hereditary neuropathy is a severe phenotype of Charcot-Marie-Tooth disease (CMT). It is characterized by early-onset (first 2 years of life), delayed motor development, slow nerve conduction velocity and severe loss of myelinated fibers in nerve biopsy.

  • Charcot–Marie–Tooth (CMT) Neuropathy Gene Panel

    Charcot-Marie-Tooth (CMT) disease is a group of hereditary neuropathies, and represents one of the most common neurological conditions, characterized by a chronic motor and sensory polyneuropathy.