Incontinentia pigmenti

Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome is a rare X-linked dominant genodermatosis related to the NF kappa B essential modulator (NEMO) gene with approximately 800 cases reported worldwide. It usually occurs in females characterized by cutaneous, skeletal, neurological, ocular and d...

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Bibliographic Details
Main Authors: Motamedi Mohammad Hosein, Lotfi Ali, Azizi Taghi, Moshref Mohammad, Farhadi Sareh
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-04-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2010;volume=53;issue=2;spage=302;epage=304;aulast=Motamedi