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ASPECTOS ETIOLOGICOS DA HIPERNASALIDADE CONSEQUENTE A PARALISIA DE PALATO MOLE - RELATO DE 6 CASOS
(1995-01-01)
The authors studied the main aspects of etiology of the palate paralysis in six children suffering from soft palate paralysis. They emphasized the importance of multidisciplinary approach in the management of patients with ...
ASPECTOS ETIOLOGICOS DA HIPERNASALIDADE CONSEQUENTE A PARALISIA DE PALATO MOLE - RELATO DE 6 CASOS
(1995-01-01)
The authors studied the main aspects of etiology of the palate paralysis in six children suffering from soft palate paralysis. They emphasized the importance of multidisciplinary approach in the management of patients with ...
Excision of an atypical case of palatal bone exostosis: a case report.
(2008-06-01)
Bone exostosis has long been described in the literature, appearing in most cases as a torus palatinus or mandibularis. These two variations are relatively common and affect approximately 30% of the world's population. ...
Excision of an atypical case of palatal bone exostosis: a case report.
(2008-06-01)
Bone exostosis has long been described in the literature, appearing in most cases as a torus palatinus or mandibularis. These two variations are relatively common and affect approximately 30% of the world's population. ...
Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome
(Elsevier, 2012)
OBJECTIVE:
Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable cause of cleft palate. ...
Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome
(Elsevier, 2012)
OBJECTIVE:
Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable cause of cleft palate. ...
The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review
(J Pediatr Genet, 2020-09-01)
The 22q11.2 deletion syndrome (22q11.2DS) is present in approximately 5 to 8% of patients with cleft lip, palate, or both (CL/P) and 75 to 80% of patients with congenital heart disease (CHD). In a literature review, we ...
Oral health-related quality of life in children in Chile treated for cleft lip and palate: A case-control approach
(American Cleft Palate Craniofacial Association, 2017)