Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome
Küçük Resim Yok
Tarih
2019
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
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-intensity conditioning prevents the morbidity/mortality in the transplantation related to myeloablative conditioning. We report on a 21-month old boy with cerebral involvement of HLH related to GS.
Açıklama
Anahtar Kelimeler
0-Belirlenecek
Kaynak
The Journal of Pediatric Research
WoS Q Değeri
N/A
Scopus Q Değeri
Cilt
6
Sayı
3
