1.
Indian Pediatr
;
2013 October; 50(10): 967-968
Article
in English
| IMSEAR
| ID: sea-170013
ABSTRACT
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.
2.
Indian Pediatr
;
2001 Aug; 38(8): 872-4
Article
in English
| IMSEAR
| ID: sea-10483