Griscelli syndrome type 3 with coexistent universal dyschromia—An uncommon association of a rare entity

Griscelli syndrome type 3 with coexistent universal dyschromia—An uncommon association of a rare entity

Griscelli syndrome type 3 is an autosomal recessive disorder caused by mutations in the melanophilin gene and does not have any mucocutaneous or systemic abnormalities other than a pigmentary dilution of skin and hair. We report a case of an 8-year-old girl who presented with silvery grey hair of sc...

Full description

Bibliographic Details
Main Authors: Sinu Rose Mathachan, Surabhi Sinha, Purnima Malhotra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Indian Dermatology Online Journal
Subjects:
grey hair
griscelli syndrome
universal dyschromia
Online Access:http://www.idoj.in/article.asp?issn=2229-5178;year=2020;volume=11;issue=5;spage=799;epage=803;aulast=Mathachan

Internet

http://www.idoj.in/article.asp?issn=2229-5178;year=2020;volume=11;issue=5;spage=799;epage=803;aulast=Mathachan

Similar Items