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Indian Pediatr ; 2003 Oct; 40(10): 1005-8
Article in English | IMSEAR | ID: sea-13377

ABSTRACT

A 6-year-old girl presented with recurrent infections, seizures, regression of milestones, silvery hair and organomegaly. A diagnosis of Griscelli syndrome with unusual features of a Dandy Walker cyst and hypergammaglobulinemia, not previously described in literature, was made. The child was treated with supportive measures.


Subject(s)
Child , Dandy-Walker Syndrome/diagnosis , Female , Humans , Hypergammaglobulinemia/diagnosis , Immunologic Deficiency Syndromes/diagnosis , Piebaldism/diagnosis , Syndrome
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