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Incontinentia pigmenti: a rare genodermatosis in a male child.

作者信息

Swamy Dinesh Kumar Narayana, Arunagirinathan Arulkumaran, Krishnakumar Revathi, Sangili Sivaraman

机构信息

Assistant Professor, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .

Associate Professor, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .

出版信息

J Clin Diagn Res. 2015 Feb;9(2):SD06-8. doi: 10.7860/JCDR/2015/12171.5561. Epub 2015 Feb 1.

Abstract

Incontinentia pigmenti is rare X-linked dominant disorder. There is no consistent expression of Incontinetia pigmenti in female child, but in male child, they always lead to death in utero. Vesicular, verrucous, hyperpigmented, and atrophic stages are the four stages of Incontinetia Pigmenti and it is uncommon for all stages to be seen in a same case. It is a rare genodermatosis, with only very few cases of male child with Incontinentia pigmenti have been reported. Thus, we report this case due to its extreme rarity and the child showed all the first 3 stages on followup.

摘要

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本文引用的文献

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