Case Reports
Griscelli syndrome: A unique pigmentary defect
Authors:
Ashish Lothe ,
Assistant Professor, Department of Pediatrics, Indira Gandhi Government Medical College and Mayo Hospital, Nagpur, IN
About Ashish
Leena Dhande
Associate Professor,, Department of Pediatrics, Indira Gandhi Government Medical College and Mayo Hospital, Nagpur, IN
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
Published on
12 Sep 2015.
Peer Reviewed
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