Apert Syndrome: A Case Report and Review of Literature
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Apert syndrome, also known as Acrocephalosyndactyly, is a rarecongenital malformation characterized by premature fusion of the cranial sutures (craniosynostosis), malformations of the skull, hands, face and feet.The inheritance of Apert syndrome is usually autosomal dominant, but sporadic cases have been reported and probably represent new mutations.This case study is reported here in order to remind clinician especially the neonatologists who are first confronted with such congenital abnormality that, this inherited condition, even though is rare as it thought to be, it should be thoroughly diagnosed....

http://file.scirp.org/Html/5-1330504_67210.htm
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