Ichthyosis, CHILD Syndrome
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Ichthyosis, CHILD Syndrome 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.
- CHILD Naevus
- CHILD Nevus
- Congenital Hemidysplasia with Ichthyosis Erythroderma and Limb Defects
- Disorders of Cornification 16
- DOC 16, Unilateral Hemidysplasia Type
- Unilateral Hemidysplasia Type
- Unilateral Ichthyosiform Erythroderma with Ipsilateral Malformations, Limb
CHILD syndrome (an acronym for congenital hemidysplasia with ichthyosiform erythroderma and limb defects) is an inherited disorder, affecting primarily women, that is characterized by ichthyosis-like skin abnormalities and limb defects on one side of the body. Other abnormalities may be present, as well.
If defects of other body organs are present, they are usually on the same side of the body as the skin and limb abnormalities.
Foundation for Ichthyosis & Related Skin Types
- 2616 N Broad Street
- Colmar, PA 18915
- Tel: (215)997-9400
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- Website: http://www.firstskinfoundation.org
Genetic and Rare Diseases (GARD) Information Center
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- Gaithersburg, MD 20898-8126
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- Fax: (301)251-4911
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- Website: http://rarediseases.info.nih.gov/GARD/
NIH/National Institute of Allergy and Infectious Diseases
- NIAID Office of Communications and Government Relations
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- Bethesda, MD 20892-9806
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- Website: http://www.niaid.nih.gov/
For a Complete Report
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".
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
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
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email email@example.com
Last Updated: 1/7/1970
Copyright 2005 National Organization for Rare Disorders, Inc.
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