29 top medical experts on Dominant Intermediate B Charcot-Marie-Tooth Disease across 3 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Dominant Intermediate B Charcot-Marie-Tooth Disease: A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with mild to moderately severe, slowly progressive usual clinical features of Charcot-Marie-Tooth disease (muscle weakness and atrophy of the distal extremities, distal sensory loss, reduced or absent deep tendon reflexes, and feet deformities). Other findings include asymptomatic neutropenia and early-onset cataracts.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: CMTDI1, CMTDIB, Type 2m Autosomal Dominant Axonal Charcot-Marie-Tooth Disease, Type 2m Axonal Charcot-Marie-Tooth Disease, With Neutropenia Dominant Intermediate B Charcot-Marie-Tooth Disease, Type 2m Axonal Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B Charcot-Marie-Tooth Neuropathy, Cmt2m
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