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

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...

Full description

Saved in:
Bibliographic Details
Main Authors: Ankur Singh (Author), Amit Garg (Author), Seema Kapoor (Author), Nita Khurana (Author), Miriam Entesarian (Author), Bianca Tesi (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available