Incontinentia pigmenti with intracranial arachnoid cyst: A case report

BACKGROUND: Incontinentia pigmenti (IP) is a rare X-linked dominant genetic disorder that can be fatal in male infants. It is a disease that affects many systems of the human body. In addition to characteristic skin changes, patients may also have pathological features of the eyes, teeth, and centra...

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Detalles Bibliográficos
Autores principales: Li, Wen-Chao, Li, Man-Li, Ding, Jiang-Wei, Wang, Lei, Wang, Shu-Ren, Wang, Yang-Yang, Xiao, Li-Fei, Sun, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403704/
https://www.ncbi.nlm.nih.gov/pubmed/36159532
http://dx.doi.org/10.12998/wjcc.v10.i23.8352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403704/
https://www.ncbi.nlm.nih.gov/pubmed/36159532
http://dx.doi.org/10.12998/wjcc.v10.i23.8352

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