177 top medical experts on Type 4E Charcot-Marie-Tooth disease across 10 countries and 12 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Type 4E Charcot-Marie-Tooth disease: Charcot-Marie-Tooth disease type 4E (CMT4E) is a congenital, hypomyelinating subtype of Charcot-Marie-Tooth disease type 4 characterized by a Dejerine-Sottas syndrome-like phenotype (incl. hypotonia and/or delayed motor development in infancy), extremely slow nerve conduction velocities, potential respiratory dysfunction, cranial nerve involvement, and the typical CMT phenotype, i.e. distal muscle weakness and atrophy, sensory loss, and foot deformity.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Type 4e Charcot-Marie-Tooth Neuropathy, Congenital Hypomyelinating Neuropathy, Congenital hypomyelinating neuropathy (CHN), severe congenital Hypomyelination, congenital hypomyelinating Neuropathy
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