Nouri-Merchaoui S, Mahdhaoui N, Methlouthi J, Zakhama R, Seboui H
Service de néonatologie, CHU Farhat-Hached, Sousse, Tunisie.
Arch Pediatr. 2011 Oct;18(10):1095-9. doi: 10.1016/j.arcped.2011.05.023. Epub 2011 Jul 26.
Incontinentia pigmenti (IP) is a rare affection inherited as X-linked dominant disease. It is usually lethal in male infants. IP can affect ectodermal tissues such as the skin, teeth, eyes, bones, and the central nervous system. Skin lesions occur mostly during the neonatal period and are characterized by a classic progression in 4 stages leading to hyperpigmentation. We report on the case of a female neonate presenting on the 3rd day of life with seizures without obvious cause, in which the diagnosis of IP was made 1 week later when skin lesions appeared.
色素失禁症(IP)是一种罕见的遗传性疾病,呈X连锁显性遗传。它通常在男婴中是致死性的。IP可影响外胚层组织,如皮肤、牙齿、眼睛、骨骼和中枢神经系统。皮肤病变大多发生在新生儿期,其特征是典型地分为4个阶段发展,最终导致色素沉着。我们报告一例女性新生儿病例,该患儿出生第3天出现无明显原因的癫痫发作,1周后出现皮肤病变时确诊为色素失禁症。