Late‐onset hemophagocytic lymphohistiocytosis with neurological presentation

Missense mutations in genes involved in familial hemophagocytic lymphohistiocytosis can delay the onset of this life‐threatening disease. In children and adults, early recognition of aspecific features as neurological symptoms is crucial as urgent treatment is required.

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Опубликовано в: :Clin Case Rep
Главные авторы: Benezech, Sarah, Walzer, Thierry, Charrier, Emily, Heidelberg, Damien, De Saint‐Basile, Geneviève, Bertrand, Yves, Belot, Alexandre
Формат: Artigo
Язык:Inglês
Опубликовано: John Wiley and Sons Inc. 2017
Предметы:
Case Reports
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5676276/
https://ncbi.nlm.nih.gov/pubmed/29152263
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1135
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