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Langerhans cell histiocytosis complicated with hemophagocytic lymphohistiocytosis in a boy with a novel XIAP mutation: A case report

RATIONALE: X-linked lymphoproliferative syndromes (XLPs) are rare, yet often fatal primary immunodeficiency diseases, which rarely manifest as Langerhans cell histiocytosis (LCH) complicated with hemophagocytic lymphohistiocytosis (HLH). Clinical data of a case of XLP-2 manifesting as LCH complicate...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Medicine (Baltimore)
Päätekijät: Guo, Xia, Li, Qiang, Gao, Ju
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wolters Kluwer Health 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6221634/
https://ncbi.nlm.nih.gov/pubmed/30383659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000013019
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