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DeCS
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Descriptor English:
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Hereditary Motor and Sensory Neuropathies
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Descriptor Spanish:
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Neuropatías Motoras y Sensoriales Hereditarias
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Descriptor Portuguese:
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Neuropatias Motoras e Sensoriais Hereditárias
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Synonyms English:
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Dejerine-Sottas Disease
HMSN
HMSN Type III
HMSN Type VII
Neuropathies, Hereditary Motor and Sensory
Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type III, Motor and Sensory Neuropathy
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Tree Number:
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C10.500.300
C10.574.500.495
C10.668.829.800.300
C16.131.666.300
C16.320.400.400
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Definition English:
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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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Indexing Annotation English:
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do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; DF: NEUROPATHIES HEREDITARY MOTOR SENSORY
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History Note English:
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2000(1989)
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Allowable Qualifiers English:
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Record Number:
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23777
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Unique Identifier:
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D015417
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Occurrence in VHL:
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Similar:
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DeCS SciELO LILACS LIS
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