Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

• Principais autores: Ersin Töret (Autor), Yılmaz Ay (Autor), Serap Aksoylar (Autor), Tuba Hilkay Karapınar (Autor), Yeşim Oymak (Autor)
• Formato: Livro
• Publicado em: Galenos Yayinevi, 2019-09-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: 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...