X-Linked Agammaglobulinemia Presenting as Neutropenia: Case Report and an Overview of Literature

X-linked agammaglobulinemia (XLA) is an inherited immunodeficiency caused by mutations in the Bruton Tyrosine Kinase (BTK) gene. Marked neutropenia can be the initial abnormal laboratory finding in patients with XLA who are presenting with their first illness. The two cases presented herein support...

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Detalles Bibliográficos
Autores principales: Lanlokun, Mosopefoluwa, Borden, Amanda, Nieves, Daime, Walter, Jolan E., Albright, Deborah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273273/
https://www.ncbi.nlm.nih.gov/pubmed/34262886
http://dx.doi.org/10.3389/fped.2021.633692

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273273/
https://www.ncbi.nlm.nih.gov/pubmed/34262886
http://dx.doi.org/10.3389/fped.2021.633692

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