Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Familial hemophagocytic lymphohistiocytosis Type 2 (FHL2) associated central nervous system (CNS) involvement is less understood in children, especially when considering neurologic manifestations as part of the initial presentation. We conducted a retrospective review of the clinical manifestations...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Front Genet
Asıl Yazarlar: Feng, Wei-xing, Yang, Xin-ying, Li, Jiu-wei, Gong, Shuai, Wu, Yun, Zhang, Wei-hua, Han, Tong-li, Zhuo, Xiu-wei, Ding, Chang-hong, Fang, Fang
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2020
Konular:
Genetics
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7064636/
https://ncbi.nlm.nih.gov/pubmed/32194620
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00126
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