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Apert syndrome: Analysis of associated brain malformations and conformational changes determined by surgical treatment
(2004-03-01)
Apert Syndrome, also called acrocephalosyndactylia type 1, is characterized by craniostenosis with early fusion of sutures of the vault and/ or cranial base, associated to mid-face hypoplasia, symmetric syndactylia of the ...
Apert syndrome: Analysis of associated brain malformations and conformational changes determined by surgical treatment
(2004-03-01)
Apert Syndrome, also called acrocephalosyndactylia type 1, is characterized by craniostenosis with early fusion of sutures of the vault and/ or cranial base, associated to mid-face hypoplasia, symmetric syndactylia of the ...
Apert syndrome: clinical and radiographic features and case report
(Pontifícia Universidade Católica do Rio Grande do Sul, 2011)
PURPOSE: Apert syndrome is a rare type I acrocephalosyndactyly syndrome characterized by craniosynostosis, severe syndactyly of the hands and feet, and dysmorphic facial features. Presents autosomal dominant inheritance ...