Incontinentia pigmenti

被引：4

作者：

Motamedi, Mohammad Hosein Kalantar ^{[1
,3
]}

Lotfi, Ali ^{[2
]}

Azizi, Taghi

Moshref, Mohammad ^{[2
]}

Farhadi, Sareh ^{[2
]}

机构：

[1] Baqiyatallah Univ Med Sci, Trauma Res Ctr, Tehran, Iran

[2] Shahid Beheshti Univ Med Sci, Dept Pathol, Tehran, Iran

[3] Azad Univ Med Sci, Tehran, Iran

来源：

INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY | 2010年 / 53卷 / 02期

关键词：

Genodermatosis; incontinentia pigmenti; skin;

D O I：

10.4103/0377-4929.64291

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

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.

引用

页码：302 / 304

页数：3

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