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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer Health
2019
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| Materias: | |
| 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 |