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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Detalles Bibliográficos
Autores principales: Walong, Edwin, Rogena, Emily, Sabai, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094674/
https://www.ncbi.nlm.nih.gov/pubmed/24996427
http://dx.doi.org/10.1186/1756-0500-7-425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094674/
https://www.ncbi.nlm.nih.gov/pubmed/24996427
http://dx.doi.org/10.1186/1756-0500-7-425

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