A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings

BACKGROUND: Cellular primary immunodeficiencies are rarely reported from Africa. DiGeorge syndrome is a commonly recognized form of a congenital T-cell deficiency. The disorder is characterized by hypoplastic or aplastic thymus, hypocalcemia, recurrent infections, and other associated congenital def...

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Detalles Bibliográficos
Autores principales: Alemayehu, Tinsae, Deribessa, Solomie Jebessa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061102/
https://www.ncbi.nlm.nih.gov/pubmed/32158567
http://dx.doi.org/10.1155/2020/8157212

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061102/
https://www.ncbi.nlm.nih.gov/pubmed/32158567
http://dx.doi.org/10.1155/2020/8157212

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