Open AccessGriscelli syndrome: A unique pigmentary defect
Author(s) -
Ashish Lothe,
Leena Dhande
Publication year - 2015
Publication title -
sri lanka journal of child health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.153
H-Index - 6
eISSN - 2386-110X
pISSN - 1391-5452
DOI - 10.4038/sljch.v44i3.8019
Subject(s) - medical journal , sri lanka , scopus , publishing , medicine , transparency (behavior) , library science , open access publishing , open access journal , family medicine , medline , political science , south asia , law , history , ethnology , computer science
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
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom