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

• Hlavní autoři: Mosopefoluwa Lanlokun (Autor), Amanda Borden (Autor), Daime Nieves (Autor), Jolan E. Walter (Autor), Deborah Albright (Autor)
• Médium: Kniha
• Vydáno: Frontiers Media S.A., 2021-06-01T00:00:00Z.
• Témata: article
• On-line přístup: Connect to this object online.

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...