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Adult onset type 2 familial hemophagocytic lymphohistiocytosis with PRF1 c.65delC/c.163C>T compound heterozygous mutations: A case report

BACKGROUND: Familial hemophagocytic lymphohistiocytosis (FHL) is a primary immunodefici-ency disease caused by gene defects. The onset of FHL in adolescents and adults may lead clinicians to ignore or even misdiagnose the disease. To the best of our knowledge, this is the first report to detail the...

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Detalles Bibliográficos
Autores principales:	Liu, Xin-Yi, Nie, Yan-Bo, Chen, Xue-Jing, Gao, Xiao-Hui, Zhai, Li-Jia, Min, Feng-Ling
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Baishideng Publishing Group Inc 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026822/ https://www.ncbi.nlm.nih.gov/pubmed/33869605 http://dx.doi.org/10.12998/wjcc.v9.i10.2289

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