Familial hemophagocytic lymphohistiocytosis in a girl with a novel homozygous mutation of STX11: A case report

RATIONALE: Familial hemophagocytic lymphohistiocytosis (FHL) is a rare fatal autosomal recessively inherited disease and can be divided into five types. The mortality of untreated patients is up to 95% and it can be healed only after immunochemotherapy for disease control and hematopoietic stem cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Xia, Jiang, Mingyan, Tang, Xue, Li, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890335/
https://www.ncbi.nlm.nih.gov/pubmed/31770233
http://dx.doi.org/10.1097/MD.0000000000018107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890335/
https://www.ncbi.nlm.nih.gov/pubmed/31770233
http://dx.doi.org/10.1097/MD.0000000000018107

Ejemplares similares