Case report: A case of incontinentia pigmenti

Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia caused by mutations in the IKBKG gene. We present a case of a 4-month-old female infant with erythematous vesicular skin lesions on the trunk and extremities. Histopathologic examination of the blisters revealed an eosinophilic infiltra...

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Detalles Bibliográficos
Autores principales: Xie, Lingfeng, Zhu, Yong, He, Liya, Yu, Bing, Wang, Jiajue, Fan, Ruiqiang, Mo, Xiumei, Zhang, Yu, Xie, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213322/
https://www.ncbi.nlm.nih.gov/pubmed/37250637
http://dx.doi.org/10.3389/fmed.2023.1164394

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213322/
https://www.ncbi.nlm.nih.gov/pubmed/37250637
http://dx.doi.org/10.3389/fmed.2023.1164394

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