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Griscelli syndrome: A unique pigmentary defect

Authors:

Ashish Lothe ,

Assistant Professor, Department of Pediatrics, Indira Gandhi Government Medical College and Mayo Hospital, Nagpur, IN
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Leena Dhande

Associate Professor,, Department of Pediatrics, Indira Gandhi Government Medical College and Mayo Hospital, Nagpur, IN
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Abstract

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

 

How to Cite: Lothe, A. and Dhande, L., 2015. Griscelli syndrome: A unique pigmentary defect. Sri Lanka Journal of Child Health, 44(3), pp.171–173. DOI: http://doi.org/10.4038/sljch.v44i3.8019
Published on 12 Sep 2015.
Peer Reviewed

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