Cargando…
Familial CNS-Isolated Hemophagocytic Lymphohistiocytosis Due to a Novel PRF1 Mutation Triggered by SARS-CoV2
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinflammatory condition that presents with fever, hepatosplenomegaly, and characteristic laboratory findings. Mutations in the perforin gene PRF1 have been implicated in cases of familial HLH (fHLH) and can cause isolate...
Autores principales: | Caldito, Natalia Gonzalez, Lorenzo, Jocelyn, Wang, Cynthia Xinzi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996508/ https://www.ncbi.nlm.nih.gov/pubmed/36911442 http://dx.doi.org/10.4103/aian.aian_719_22 |
Ejemplares similares
-
Familial Hemophagocytic Lymphohistiocytosis Secondary to PRF1 Mutation
por: Alfaraidi, Albaraa T., et al.
Publicado: (2021) -
Pediatric CNS-isolated hemophagocytic lymphohistiocytosis
por: Benson, Leslie A., et al.
Publicado: (2019) -
Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients
por: Feng, Wei-xing, et al.
Publicado: (2020) -
A novel PRF1 gene mutation in a fatal neonate case with type 2 familial hemophagocytic lymphohistiocytosis
por: Kim, Jae Yeon, et al.
Publicado: (2014) -
Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid
por: Mian, Agrima, et al.
Publicado: (2019)