Griscelli Syndrome Type 2: A Rare Case With Apparently Normal Skin and Hair Pigmentation

Griscelli Syndrome Type 2: A Rare Case With Apparently Normal Skin and Hair Pigmentation

Griscelli syndrome (GS) is a rare autosomal recessive disease that affects hair, skin, and immune system. Here, we describe an 8.5-month-old infant with multiple admissions due to fever, petechial purpura, and several recurrent vomiting episodes with a presumptive diagnosis of recurrent sepsis. He...

Full description

Bibliographic Details
Main Authors: Ahmad Bahrami, Alireza Nateghian, Shima Salehi, Gholamreza Bahoush, Saeed Talebi, Saeide Ghasemi, Sepideh Razi, Nima Rezaei
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2020-06-01
Series:Acta Medica Iranica
Subjects:
Griscelli syndrome
Pigmentation disorder
Immunodeficiency
Hemophagocytic lymphohistiocytosis
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/7825

Internet

https://acta.tums.ac.ir/index.php/acta/article/view/7825

Similar Items