10 top medical experts on Type I Distal Hereditary Motor Neuronopathy across 1 countries and 1 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Type I Distal Hereditary Motor Neuronopathy: Distal hereditary motor neuropathy type 1 is a rare neuromuscular disease characterized by slowly-progressive lower limb muscular weakness and atrophy, without sensory impairment. Additional clinical features may include pes cavus, hammertoe and increased muscle tone.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: I Spinal Charcot-Marie-Tooth Disease, Type I Distal Hereditary Motor Neuropathy, I Autosomal Dominant Juvenile Distal Spinal Muscular Atrophy
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