Griscelli syndrome Type 2: A report of rare case

• Main Authors: Chandramohan Kudligi (Author), Pradeep Vittal Bhagwat (Author), Mary Zothanpuii Chhangte (Author), Vidya Kuntoji (Author), Sujata Giriyan (Author), Veena Andanappanavar (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2017-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Griscelli syndrome (GS) is a rare autosomal recessive disorder characterized by pigmentary dilution of the hair and skin. Three different types (1-3) caused by mutation in three different genes have been described. GS2 is characterized by partial albinism, immunodeficiency, organomegaly, and hemopha...