INCONTINENTIA PIGMENTI
Welcome to this web site developed by the Incontinentia
Pigmenti International Foundation to help patients,
families, researchers and health care professionals to
understand IP and its effects. The Foundation offers
information about the disorder, patient and family support,
as well as research support.
Incontinentia Pigmenti (IP) is a genetic disease of
the skin, hair, teeth and central nervous system. The
condition was named because of the way the skin looks under
the microscope. "Bloch-Sulzberger Syndrome" is another name
commonly used for IP. Other names are: Bloch-Siemens
incontinentia pigmenti, melanoblastosis cutis linearis, and
pigmented dermatosis, Siemens-Bloch type.
Please follow the links to the side or below to learn more about IP and the Foundation:
Inheritance
Physical Findings
Diagnosis
Eye Exams in Infants
IP in Males
THE NEMO GENE
Genetics
Gene Discovery
IP Consortium
Benefits of Gene Discovery
Effects of NEMO Gene Defects
Mutation types
Next Steps
Potential for Treatment?
Testing NEMO for Mutations
More Information
Director's Letter
Scientific Advisory Board
IP Support Groups
IP Bibliography
Newsletters
Join the IPIF
Contact the IPIF
This site in other languages (not available yet):
French
German
Italian
Portuguese
Spanish