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Primary immunodeficiency diagnosed at autopsy: a case report
BACKGROUND: DiGeorge syndrome may manifest as severe immunodeficiency diagnosed at infancy. The diagnosis of primary immunodeficiency is based on characteristic clinical features, immunophenotyping by flow cytometry, molecular diagnostics and functional lymphocyte evaluation. At autopsy, gross evalu...
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4094674/ https://ncbi.nlm.nih.gov/pubmed/24996427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-7-425 |
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