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Indian Pediatr ; 2013 October; 50(10): 967-968
Artigo em Inglês | IMSEAR | ID: sea-170013

RESUMO

Greig cephalopolysyndactyly syndrome is a rare genetic disorder, with an autosomal dominant inheritance and consisting of a triad of polysyndactyly, macrocephaly and hypertelorism. Crossed polydactyly is a finding characteristically associated with this syndrome. We report a one and half year old male child who presented with classic clinical features and family history diagnostic of the above syndrome.

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