Ichthyosis, CHILD Syndrome

Ichthyosis, CHILD Syndrome
Synonyms
Disorder Subdivisions
General Discussion
Resources
For a Complete Report

Content provided by National Organization for Rare Disorders

Important

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.

Synonyms

Congenital Hemidysplasia with Ichthyosis Erythroderma and Limb Defects
DOC 16, Unilateral Hemidysplasia Type
Disorders of Cornification 16
Unilateral Hemidysplasia Type
Unilateral Ichthyosiform Erythroderma with Ipsilateral Malformations, Limb
CHILD Nevus
CHILD Naevus

Disorder Subdivisions

None

General Discussion

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.

Resources

Foundation for Ichthyosis & Related Skin Types

1364 Welsh Road G2

North Wales, PA 19454

Tel: (215)619-0670

Fax: (215)619-0780

Tel: (800)545-3286

Email: info@scalyskin.org

Internet: http://www.scalyskin.org

NIH/National Institute of Allergy and Infectious Diseases

6610 Rockledge Drive

MSC 6612

Bethesda, MD 20892-6612

Tel: (301)496-5717

Fax: (301)402-3573

TDD: (800)877-8339

Internet: http://www.niaid.nih.gov/

For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html

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 orphan@rarediseases.org

Last Updated: 4/14/2005

Copyright 1988, 1989, 1992, 1993, 1997, 2005 National Organization for Rare Disorders, Inc.

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Last updated:	April 14, 2005

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