About The Medical Condition Dejerine-Sottas Disease
Find the definition of the medical term Dejerine-Sottas Disease. Dejerine-Sottas Disease defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Dejerine-Sottas Disease
| Dejerine-Sottas Disease Medical Condition |
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What's The Definition Of The Medical Condition Dejerine-Sottas Disease?
A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy, HMSN IV refers to REFSUM DISEASE, HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)
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