It is possible that the main title of the report Incontinentia Pigmenti 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.
- Bloch-Siemens-Sulzberger Syndrome
- Bloch-Sulzberger Syndrome
- Bloch-Siemens Incontinentia Pigmenti Melanoblastosis Cutis Linearis
- Pigmented Dermatosis, Siemens-Bloch type
Incontinentia Pigmenti (IP) is a rare genetic dermatological disorder affecting the skin, hair, teeth, and central nervous system. Progressive skin changes occur in four stages, the first of which appears in early infancy or is present at birth. IP is inherited as an X-linked dominant trait.
National Foundation for Ectodermal Dysplasias
410 East Main Street
Mascoutah, IL 62258-0114
March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
Incontinentia Pigmenti International Foundation
30 East 72nd Street
New York, NY 10021
NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
One AMS Circle
Bethesda, MD 20892-3675
MUMS National Parent-to-Parent Network
150 Custer Court
Green Bay, WI 54301-1243
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
PO Box 241956
Los Angeles, CA 90024
Ectodermal Dysplasia Society
Unit 1 Maida Vale Business Centre
Gloucestershire, GL53 9ER
Tel: +44 (0) 1242 261332
Fax: +44 (0) 1242 261332
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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: 5/7/2008
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