Neuropathy, Congenital Hypomyelination
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Neuropathy, Congenital Hypomyelination is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Charcot-Marie-Tooth Type 4E
- Congenital Dysmyelinating Neuropathy
- Congenital Hypomyelinating Polyneuropathy
- Congenital Hypomyelination
- Congenital Hypomyelination Neuropathy
- Congenital Hypomyelination (Onion Bulb), Polyneuropathy
- Congenital Neuropathy caused by Hypomyelination
- Hypomyelination Neuropathy
Congenital hypomyelination neuropathy (CHN) is a neurological disorder present at birth. Major symptoms may include respiratory difficulty, muscle weakness and incoordination, poor muscle tone (neonatal hypotonia), absence of reflexes (areflexia), difficulty in walking (ataxia), and/or impaired abilities to feel or move part of the body.
American Autoimmune & Related Diseases
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Genetic and Rare Diseases (GARD) Information Center
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March of Dimes Birth Defects Foundation
- 1275 Mamaroneck Avenue
- White Plains, NY 10605
- Tel: (914)997-4488
- Fax: (914)997-4763
- Website: http://www.marchofdimes.com
NIH/National Institute of Neurological Disorders and Stroke
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- Bethesda, MD 20824
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- Fax: (301)402-2186
- Tel: (800)352-9424
- Website: http://www.ninds.nih.gov/
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This is an abstract of a report from the National Organization for Rare Disorders (NORD). A copy of the complete report can be downloaded free from the NORD website for registered users. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational therapies (if available), and references from medical literature. For a full-text version of this topic, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
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It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
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Last Updated: 1/5/1970
Copyright 2007 National Organization for Rare Disorders, Inc.
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