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...

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Main Authors: Sinu Rose Mathachan (Author), Surabhi Sinha (Author), Purnima Malhotra (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2020-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available