Three Cases of Pigmentary Incontinence and Literature Review
Background: Incontinentia pigmenti (IP) is a rare X-linked dominantly inherited genetic skin disorder in which most male infants cannot survive. The clinical manifestation is mainly characterized by a characteristic rash, which may also involve multiple extracutaneous organs. Case Presentation: We...
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Language: | English |
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Mazandaran University of Medical Sciences
2024-10-01
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Series: | Journal of Pediatrics Review |
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Online Access: | http://jpr.mazums.ac.ir/article-1-658-en.pdf |
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author | Yunfeng Zhang Yuan Wang Jinpu Zhang Na Song |
author_facet | Yunfeng Zhang Yuan Wang Jinpu Zhang Na Song |
author_sort | Yunfeng Zhang |
collection | DOAJ |
description | Background: Incontinentia pigmenti (IP) is a rare X-linked dominantly inherited genetic skin disorder in which most male infants cannot survive. The clinical manifestation is mainly characterized by a characteristic rash, which may also involve multiple extracutaneous organs.
Case Presentation: We reported three children with pigmentary incontinence, and a literature review was conducted to elaborate on the clinical manifestations of various systems in patients with IP.
Conclusions: IP is a disease that involves multiple systems and patients with IP are likely to develop serious ocular and neurologic complications. Once diagnosed, neurologists, ophthalmologists, and dentists must consult and evaluate patients multidisciplinaryly. Early intervention and adherence to lifelong follow-up are needed. |
format | Article |
id | doaj-art-f5c46d1799974188b7f20c8b9eecc417 |
institution | Kabale University |
issn | 2322-4398 2322-4401 |
language | English |
publishDate | 2024-10-01 |
publisher | Mazandaran University of Medical Sciences |
record_format | Article |
series | Journal of Pediatrics Review |
spelling | doaj-art-f5c46d1799974188b7f20c8b9eecc4172025-01-25T13:28:52ZengMazandaran University of Medical SciencesJournal of Pediatrics Review2322-43982322-44012024-10-01124359368Three Cases of Pigmentary Incontinence and Literature ReviewYunfeng Zhang0Yuan Wang1Jinpu Zhang2Na Song3 Department of Neonatology, The Second Hospital of Jilin University, Changchun, China. Department of Neonatology, The Second Hospital of Jilin University, Changchun, China. Department of Neonatology, The Second Hospital of Jilin University, Changchun, China. Department of Neonatology, The Second Hospital of Jilin University, Changchun, China. Background: Incontinentia pigmenti (IP) is a rare X-linked dominantly inherited genetic skin disorder in which most male infants cannot survive. The clinical manifestation is mainly characterized by a characteristic rash, which may also involve multiple extracutaneous organs. Case Presentation: We reported three children with pigmentary incontinence, and a literature review was conducted to elaborate on the clinical manifestations of various systems in patients with IP. Conclusions: IP is a disease that involves multiple systems and patients with IP are likely to develop serious ocular and neurologic complications. Once diagnosed, neurologists, ophthalmologists, and dentists must consult and evaluate patients multidisciplinaryly. Early intervention and adherence to lifelong follow-up are needed.http://jpr.mazums.ac.ir/article-1-658-en.pdfincontinentia pigmentiretinopathyneonataldiagnosisscreeningfollow-up |
spellingShingle | Yunfeng Zhang Yuan Wang Jinpu Zhang Na Song Three Cases of Pigmentary Incontinence and Literature Review Journal of Pediatrics Review incontinentia pigmenti retinopathy neonatal diagnosis screening follow-up |
title | Three Cases of Pigmentary Incontinence and Literature Review |
title_full | Three Cases of Pigmentary Incontinence and Literature Review |
title_fullStr | Three Cases of Pigmentary Incontinence and Literature Review |
title_full_unstemmed | Three Cases of Pigmentary Incontinence and Literature Review |
title_short | Three Cases of Pigmentary Incontinence and Literature Review |
title_sort | three cases of pigmentary incontinence and literature review |
topic | incontinentia pigmenti retinopathy neonatal diagnosis screening follow-up |
url | http://jpr.mazums.ac.ir/article-1-658-en.pdf |
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