Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

• Asıl Yazarlar: Ersin Töret (Yazar), Yılmaz Ay (Yazar), Serap Aksoylar (Yazar), Tuba Hilkay Karapınar (Yazar), Yeşim Oymak (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Galenos Yayinevi, 2019-09-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Type II Griscelli Syndrome (GS) is caused by a mutation in the RAB27A gene and usually manifests with silvery-gray hair, immune deficiency and the development of hemophagocytic lymphohistiocytosis (HLH). A hematopoietic stem cell transplantation is the curative treatment for HLH and reduced-intensit...