Central nervous system anomalies in 41 Chinese children incontinentia pigmenti

Central nervous system anomalies in 41 Chinese children incontinentia pigmenti

Abstract Introduction Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia caused by a defect in the IKBKG gene. The pathogenesis of central nervous system injury is believed to be related to microvascular ischemia. Currently, few treatment strategies are available for the inflammatory ph...

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Bibliographic Details
Main Authors: Li Yin, Zhengyuan Li, Wenjuan Zhan, Yuanjie Kang, Qian Tian, Dan Li, Huifang Zhang
Format: Article
Language:English
Published: BMC 2024-05-01
Series:BMC Neuroscience
Subjects:
Incontinentia pigmenti
Cerebral ischemia
IKBKG gene
Online Access:https://doi.org/10.1186/s12868-024-00872-1

Internet

https://doi.org/10.1186/s12868-024-00872-1

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