Ichthyosis, Netherton Syndrome

Ichthyosis, Netherton 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, Netherton 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

Comel-Netherton Syndrome
Ichthyosis Linearis Circumflexa

Disorder Subdivisions

None

General Discussion

Netherton syndrome is a rare hereditary disorder characterized by scaling skin, hair anomalies, increased susceptibility to atopic eczema (a skin condition that can result in dry, red and flaky skin), elevated IgE levels, and other related symptoms. Netherton syndrome is inherited as an autosomal recessive trait.

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 Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse

1 AMS Circle

Bethesda, MD 20892-3675

USA

Tel: 3014954484

Fax: 3017186366

Tel: 8772264267

TDD: 3015652966

Email: NIAMSinfo@mail.nih.gov

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

National Registry for Ichthyosis and Related Disorders

University of Washington

Dermatology Department, Box 356524

1959 N.E. Pacific

Seattle, WA 98195-6524

Tel: (206)616-3179

Fax: (206)616-6793

Tel: (800)595-1265

Email: ichreg@u.washington.edu

Internet: http://www.skinregistry.org

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: 4/5/2005

Copyright 1988, 1989, 1993, 1997, 1999, 2004, 2005 National Organization for Rare Disorders, Inc.

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Last updated:	April 05, 2005

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