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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.
Uloženo v:
| Vydáno v: | Clin Case Rep |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2017
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| 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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