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• W2341485576 abstract "Apert syndrome is a rare autosomal dominant genetic disorder characterized by irregular craniosynostosis, symmetric syndactylia of hands and feet, and mid-line hypoplasia. In this paper, we present a case with typical face appearance consisting of acrocephaly, high and prominent forehed, antimogoloid axis, hypertelorism, proptosis, mid-facial hypoplasia, symmetric syndactylia of hands and feet, many synostosis on both hands and cutaneous syndactylies, cerebellar hypoplasia, cervical vertebra fusion, and to discuss the clinical features of Apert syndrome." @default.
• W2341485576 created "2016-06-24" @default.
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• W2341485576 date "2009-01-01" @default.
• W2341485576 modified "2023-09-26" @default.
• W2341485576 title "ARAÞTIRMALAR (Research Reports)" @default.
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