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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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Podrobná bibliografie
Vydáno v:Clin Case Rep
Hlavní autoři: Benezech, Sarah, Walzer, Thierry, Charrier, Emily, Heidelberg, Damien, De Saint‐Basile, Geneviève, Bertrand, Yves, Belot, Alexandre
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2017
Témata:
On-line přístup: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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