Recurrent Infections in an Ethiopian Boy with Autosomal Recessive Major Histocompatibility Complex Type I Deficiency: a Case Report on a Very Rare Primary Immunodeficiency Disorder and a Review of Principles in Evaluation and Management

Little is known about major histocompatibility complex type I deficiency, a rare form of primary immunodeficiency. This report describes the presentation of a three-year-old Ethiopian boy with recurrent sinopulmonary infections and genetic analysis showing him having autosomal recessive major histoc...

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Detalles Bibliográficos
Autores principales: Alemayehu, Tinsae, Gebeyehu, Netsanet Azene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559549/
https://www.ncbi.nlm.nih.gov/pubmed/36229627
http://dx.doi.org/10.1007/s10875-022-01381-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559549/
https://www.ncbi.nlm.nih.gov/pubmed/36229627
http://dx.doi.org/10.1007/s10875-022-01381-8

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