Griscelli syndrome: A unique pigmentary defect
By: Ashish Lothe and Leena Dhande
Open Access
|Sep 2015Abstract
Griscelli syndrome (GS) is rare autosomal recessive disorder with pigmentary dilution, immunodeficiency and neurological involvement1,2. We report a child with classical features of GS and pathognomonic histopathological features of skin and hair.
Sri Lanka Journal of Child Health, 2015; 44(3): 171-173
DOI: https://doi.org/10.4038/sljch.v44i3.8019 | Journal eISSN: 2386-110X
Language: English
Page range: 171 - 173
Published on: Sep 12, 2015
Published by: Sri Lanka College of Paediatricians
In partnership with: Paradigm Publishing Services
© 2015 Ashish Lothe, Leena Dhande, published by Sri Lanka College of Paediatricians
This work is licensed under the Creative Commons License.