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Griscelli Syndrome: A Case Report

Griscelli syndrome (GS) is a rare autosomal recessive immune deficiency disorder that presents with pigmentary dilution of the skin and hair, recurrent skin and pulmonary infections, neurologic problems, hypogammaglobulinemia, and variable cellular immunodeficiency. Three mutations have been describ...

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Detalhes bibliográficos
Publicado no:Iran J Child Neurol
Main Authors: MANSOURI NEJAD, Seyed Ebrahim, YAZDAN PANAH, Mohammad Javad, TAYYEBI MEIBODI, Naser, ASHRAF ZADEH, Farah, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran, ESLAMIEH, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: Shahid Beheshti University of Medical Sciences 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4307372/
https://ncbi.nlm.nih.gov/pubmed/25657774
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