 |
|
Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
| Enter a medical term |
| Hereditary Sensory and Motor Neuropathy | Legal notice |
Other terms
Neuropathies, Hereditary Motor and Sensory,HMSN,Hereditary Motor and Sensory Neuropathies,Herditary Sensory and Motor Neuropathy,HMSN Type III,HMSN Type IIIs,Hereditary, Type III, Motor and Sensory Neuropathy,Dejerine-Sottas Disease,Dejerine Sottas Disease,Disease, Dejerine-Sottas,Hereditary, Type VII, Motor and Sensory Neuropathy,HMSN Type VII,HMSN Type VIIs,Type VII, HMSN
Description
Hereditary Sensory and Motor Neuropathy: 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)
Pervious tree
Next tree
- Charcot-Marie-Tooth Disease
- Refsum Disease
- Spastic Paraplegia, Hereditary
- Giant Axonal Neuropathy
- Alstrom Syndrome
Other locations in tree
- Heredodegenerative Disorders, Nervous System
- Polyneuropathies
- Nervous System Malformations
- Heredodegenerative Disorders, Nervous System
Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
Neither the United States Government, nor any of its agencies, contractors, subcontractors or employees makes any warranties, expressed or implied, with respect to data contained in the database, and, furthermore, assumes no legal liability for any party's use, or the results of such use, of any part of the database.
You will not assert any proprietary rights to any portion of the database, or represent the database or any part thereof to anyone as other than a United States Government database.
The MeSH data carry an international copyright outside the United States, its Territories or Possessions. These terms and conditions are in effect as long as the user retains any of the MeSH data obtained from this site.