1 publication

• Published Subscription 13 Sep 2018

  Griscelli Syndrome Type 2: A Case Report on Its Diagnosis and Management

  By Ansu Ann Mathew, Iswar Hazarika

  Abstract: Griscelli syndrome (GS) is an autosomal recessive disorder which is very rare and is characterized by dilution of pigments and variable immunodeficiency. Researchers have identified three types of this disorder which are distinguished by their genetic cause and pattern of signs and symptoms: Type 1, Type 2 and Type 3, caused by the mutation of MYO5A, RAB27A and MLPH genes respectively. Subtype 2 being the most common, is characterized by …

  Published in Research and Reviews : A Journal of Immunology · Vol. 8, Issue 2, 2018 · pp. 5–7 Read article →