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X-Linked Inhibitor of Apoptosis (XIAP) deficiency presenting as hemophagocytic lymphohistiocytosis triggered by drug allergy

X-linked inhibitor of apoptosis (XIAP) deficiency is a primary immunodeficiency associated with recurrent hemophagocytic lymphohistiocytosis (HLH) episodes. The clinical phenotypes of XIAP deficiency vary, ranging from splenomegaly to life-threatening inflammation. We report a case of XIAP deficienc...

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Hlavní autoři: Amer Khojah, Ameera Bukhari, Aaruni Khanolkar, Imad Khojah, Abigail Lang
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2023-12-01
Edice:Clinical Immunology Communications
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On-line přístup:http://www.sciencedirect.com/science/article/pii/S2772613423000082
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