Hematopoietic stem cell transplantation in children with Griscelli Syndrome type 2: Experience and outcomes

Griscelli syndrome is a rare autosomal recessive inherited disorder characterized by hypopigmentation, silver colored hair, and associated immunological deficiency, which proves fatal in the absence of timely intervention. Our patients diagnosed with Griscelli syndrome-2 presented with fever, hepato...

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Detalhes bibliográficos

Principais autores:	Devika Gupta, Deepshi Thakral, Sameer Bakhshi, Sushil Kumar Kabra, Dipendra Kumar Mitra
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wolters Kluwer Medknow Publications 2019-01-01
coleção:	Indian Journal of Pathology and Microbiology
Assuntos:	Griscelli syndrome Hemophagocytic lymphohistiocytosis Hematopoietic stem cell transplant RAB27A gene
Acesso em linha:	http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=2;spage=279;epage=282;aulast=Gupta
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