(2010) Incontinentia pigmenti. Indian Journal of Pathology and Microbiology. pp. 302-304. ISSN 0377-4929
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Abstract
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 dental abnormalities as well as an increased risk of childhood malignancies. Herein, we report a case of IP in a 14-year-old girl emphasizing early diagnosis and adding to the current literature on the subject.
| Item Type: | Article |
|---|---|
| Keywords: | Genodermatosis incontinentia pigmenti skin Pathology |
| Divisions: | |
| Page Range: | pp. 302-304 |
| Journal or Publication Title: | Indian Journal of Pathology and Microbiology |
| Journal Index: | ISI |
| Volume: | 53 |
| Number: | 2 |
| Identification Number: | https://doi.org/10.4103/0377-4929.64291 |
| ISSN: | 0377-4929 |
| Depositing User: | مهندس مهدی شریفی |
| URI: | http://eprints.bmsu.ac.ir/id/eprint/6744 |
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