Griscelli syndrome Type 2: A report of rare case

Griscelli syndrome Type 2: A report of rare case

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...

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Bibliographic Details
Main Authors: Chandramohan Kudligi, Pradeep Vittal Bhagwat, Mary Zothanpuii Chhangte, Vidya Kuntoji, Sujata Giriyan, Veena Andanappanavar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Clinical Dermatology Review
Subjects:
griscelli syndrome
melanin clumps
nystagmus
silvery hair
Online Access:http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2017;volume=1;issue=2;spage=65;epage=68;aulast=Kudligi

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http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2017;volume=1;issue=2;spage=65;epage=68;aulast=Kudligi

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