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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Bibliographische Detailangaben
Veröffentlicht in:Iran J Child Neurol
Hauptverfasser: MANSOURI NEJAD, Seyed Ebrahim, YAZDAN PANAH, Mohammad Javad, TAYYEBI MEIBODI, Naser, ASHRAF ZADEH, Farah, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran, ESLAMIEH, Hossein
Format: Artigo
Sprache:Inglês
Veröffentlicht: Shahid Beheshti University of Medical Sciences 2014
Schlagworte:
Case Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4307372/
https://ncbi.nlm.nih.gov/pubmed/25657774
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