Structured Summary
Abstract
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)
MeSH Record
Classification
Related Concepts
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MeSH Record
Synonyms
33 entry terms
- HMSN
- Herditary Sensory and Motor Neuropathy
- Hereditary Motor and Sensory Neuropathies
- Hereditary Motor and Sensory Neuropathy
- Neuropathies, Hereditary Motor and Sensory
- CMT4f
- Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
- Charcot-Marie-Tooth Disease, Type 3
- Dejerine-Sottas Disease
- Dejerine-Sottas Neuropathy
- Dejerine-Sottas Syndrome
- HMN (Hereditary Motor Neuropathy) Proximal Type I
- HMSN Type III
- HMSN Type VII
- HMSN3
- Hereditary Motor and Sensory Neuropathy 3
- Hereditary Motor and Sensory Neuropathy Type III
- Hereditary, Type III, Motor and Sensory Neuropathy
- Hereditary, Type VII, Motor and Sensory Neuropathy
- Hypertrophic Neuropathy of Dejerine-Sottas
- Proximal Hereditary Motor Neuropathy Type I
- Charcot Marie Tooth Disease, Type 3
- Dejerine Sottas Disease
- Dejerine Sottas Neuropathy
- Dejerine Sottas Syndrome
- Dejerine-Sottas Hypertrophic Neuropathy
- Disease, Dejerine-Sottas
- HMSN Type IIIs
- HMSN Type VIIs
- Hypertrophic Neuropathy of Dejerine Sottas
- Neuropathy, Dejerine-Sottas
- Syndrome, Dejerine-Sottas
- Type VII, HMSN
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES
MeSH Record
History Note
2000(1989); for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I use SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025
MeSH Record
Previous Indexing
- Charcot-Marie Disease (1975-1988)
- Muscular Atrophy (1972-1988)
- Neuromuscular Diseases (1979-1988)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Hereditary Sensory and Motor Neuropathy. Medical Subject Headings (MeSH). 2026. Unique ID D015417. http://id.nlm.nih.gov/mesh/2026/D015417
- Hereditary Sensory and Motor Neuropathy. In: Wikipedia. https://en.wikipedia.org/wiki/Hereditary_motor_and_sensory_neuropathy
- Hereditary Sensory and Motor Neuropathy. In: Wikidata. https://www.wikidata.org/wiki/Q15270307