Case Report: Multiple peripheral nerve demyelinating lesions and cerebrovascular injury which resulted in extensive cerebral infarction in a XLP1 patient without EBV infection

X-linked lymphocytic proliferative disease type 1 (XLP1) is a primary immune deficiency caused by genetic alterations in the SH2D1A gene, exhibiting a wide variety of severe clinical phenotypes and high mortality. We present the case of a 16-year-old male patient diagnosed with XLP1 who suffered fro...

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Asıl Yazarlar:	Jiaxun Li, Dongcan Mo, Luyu Lv, Fuling Huang, Binyan Wu, Chunjuan He, Hao Wu, Wenpeng Pang, Yan Li, Liping Guo, Man Luo
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	Frontiers Media S.A. 2025-05-01
Seri Bilgileri:	Frontiers in Immunology
Konular:	X-linked lymphoproliferative syndrome type 1 multiple peripheral nerve demyelinating lesions cerebral infarction SH2D1A gene case report
Online Erişim:	https://www.frontiersin.org/articles/10.3389/fimmu.2025.1580909/full
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