Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric Center

Objective: Inborn errors of immunity (IEIs) are caused by deficiencies or functional abnormalities in the immune system, leading to increased susceptibility to infections, autoimmunity, autoinflammatory diseases, allergies, and/or malignancies. Primary hemophagocytic lymphohistiocytosis (HLH) arises...

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Autors principals:	Ahmet Gökcan Öztürk, Zehra Şule Haskoloğlu, Hasan Fatih Çakmaklı, Candan İslamoğlu, Talia İleri, Elif İnce, Sonay İncesoy Özdemir, Handan Uğur Dinçaslan, Nurdan Taçyıldız, Emel Cabı Ünal, Figen Doğu, Mehmet Ertem, Aydan İkincioğulları
Format:	Artigo
Idioma:	Inglês
Publicat:	Turkish Society of Hematology 2026-03-01
Col·lecció:	Turkish Journal of Hematology
Matèries:	primary immunodeficiency hemophagocytic lymphohistiocytosis hematopoietic stem cell transplantation
Accés en línia:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-10438
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