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Publication Details
AFRICAN RESEARCH NEXUS
SHINING A SPOTLIGHT ON AFRICAN RESEARCH
medicine
Incontinentia pigmenti: A case study
Journal Francais d'Ophtalmologie, Volume 30, No. 8, Year 2007
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Description
Incontinentia pigmenti is a rare hereditary, dominant, X-linked disorder. It involves the skin, the teeth, the eyes and the central nervous system. The case we report is an infant girl aged 2 months. She had typical skin lesions associated with severe impairment of her left eye. We comment on the clinical, histological, genetic, and therapeutic characteristics of this rare disease. Ophthalmologic examination should be made early in order to diagnose ocular involvement at an early stage of the disease to provide for greater treatment possibilities. © 2007. Elsevier Masson SAS.
Authors & Co-Authors
Tnacheri Ouazzani, B.
Morocco, Rabat
Hôpital Des Spécialités
Guedira, K.
Morocco, Rabat
Hôpital Des Spécialités
Dali, H.
Morocco, Rabat
Hôpital Des Spécialités
Laghmari, Mina
Morocco, Rabat
Hôpital Des Spécialités
Ibrahimy, Wafaa
Morocco, Rabat
Hôpital Des Spécialités
Daoudi, Rajaa
Morocco, Rabat
Hôpital Des Spécialités
Sefiani, Abdelaziz
Morocco, Agdal Rabat
Institut National D'hygiène
Chakir, M.
Morocco, Rabat
Hôpital Des Spécialités
Jiddane, Mohammed
Morocco, Rabat
Hôpital Des Spécialités
Mohcine, Z.
Morocco, Rabat
Hôpital Des Spécialités
Statistics
Citations: 10
Authors: 10
Affiliations: 2
Identifiers
Doi:
10.1016/s0181-5512(07)92622-4
ISSN:
01815512
Research Areas
Genetics And Genomics
Health System And Policy
Maternal And Child Health
Study Design
Case Study
Study Approach
Qualitative
Participants Gender
Female