An Indian boy with griscelli syndrome type 2: Case report and review of literature

• Main Authors: Ankur Singh (Author), Amit Garg (Author), Seema Kapoor (Author), Nita Khurana (Author), Miriam Entesarian (Author), Bianca Tesi (Author)
• 格式: 图书
• 出版: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
• 主题: article
• 在线阅读: Connect to this object online.

Griscelli syndrome 2 is a rare autosomal recessive disorder of pigmentary dilution of hair, skin, splenohepatomegaly, pancytopenia, immune and neurologic dysfunction. Clinical course is characterized by recurrent infection triggered by uncontrolled T-lymphocyte and macrophage activation, called hemo...