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Comparison of periodontal parameters in individuals with syndromic craniosynostosis
(Faculdade De Odontologia De Bauru - USP, 2009)
Craniosynostosis syndromes are characterized by premature closure of one or more cranial sutures, associated with other malformations, the most frequent of which are the Crouzon and Apert syndromes. Few studies in the ...
Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene
(Biomed Central Ltd, 2012-01-19)
Background: the majority of Marfan syndrome (MFS) cases is caused by mutations in the fibrillin-1 gene (FBN1), mapped to chromosome 15q21.1. Only few reports on deletions including the whole FBN1 gene, detected by molecular ...
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 ...
Manejo do paciente no período perioperatório em neurocirurgia pediátrica
(Associação Médica Brasileira, 2012-06-01)
OBJECTIVES: To describe the main pathophysiological differences in neurosurgical procedures between children and adults; the main complications and adverse events resulting from pediatric neurosurgery reported in studies; ...