Incontinentia pigmenti
2010
Motamedi Mohammad Hosein | Lotfi Ali | Azizi Taghi | Moshref Mohammad | Farhadi Sareh
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.
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书目信息
Indian Journal of Pathology and Microbiology
卷
53
期
2
页码
302
- 304
ISSN
0377-4929 | 0974-5130
出版者
Wolters Kluwer Medknow Publications
其它主题
Genodermatosis; Incontinentia pigmenti
语言
英语
2024-12-11
DOAJ