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.

Detalles Bibliográficos
Autores principales: Benezech, Sarah, Walzer, Thierry, Charrier, Emily, Heidelberg, Damien, De Saint‐Basile, Geneviève, Bertrand, Yves, Belot, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676276/
https://www.ncbi.nlm.nih.gov/pubmed/29152263
http://dx.doi.org/10.1002/ccr3.1135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676276/
https://www.ncbi.nlm.nih.gov/pubmed/29152263
http://dx.doi.org/10.1002/ccr3.1135

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