Familial hemophagocytic phohistiocytosis induced by PRF1 mutation with neurologic manifestations as the initial clinical presentations: A case report

To investigate the clinical characteristics of familial hemophagocytic phohistiocytosis (FHL) induced by PRF1 gene mutation and with central nervous injury as the initial presentation. CASE PRESENTATION: Herein, we presented 2 cases of a familial hemophagocytic syndrome caused by PRF1 gene mutation...

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Detalles Bibliográficos
Autores principales: You, Yang, Wu, Wenjuan, Li, Baoguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313311/
https://www.ncbi.nlm.nih.gov/pubmed/37390248
http://dx.doi.org/10.1097/MD.0000000000034198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313311/
https://www.ncbi.nlm.nih.gov/pubmed/37390248
http://dx.doi.org/10.1097/MD.0000000000034198

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