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XIAP deficiency and MEFV variants resulting in an autoinflammatory lymphoproliferative syndrome
A 16-year-old boy of Caucasian ethnicity was evaluated for recurrent febrile episodes occurring during most of his life without establishment of any microbial aetiology. During febrile episodes he developed extensive splenomegaly, lymphadenopathy, anaemia, severe abdominal pain and general malaise....
Tallennettuna:
| Julkaisussa: | BMJ Case Rep |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5051366/ https://ncbi.nlm.nih.gov/pubmed/27681353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2016-216922 |
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