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Now showing items 21-30 of 128
Craneosinostosis, una perspectiva pediátrica
(Sociedad Chilena de Pediatría, 2020)
La craneosinostosis se define como el cierre prematuro de una o más suturas del cráneo, que se
manifiesta por una forma anormal de la cabeza. Es una condición infrecuente, pero requiere ser
reconocida y derivada oportunamente ...
Apert Syndrome: Report of a Case With Emphasis on Craniofacial and Genetic Features
(Amer Acad Pediatric DentistryChicagoEUA, 2008)
Syndromic craniosynostosis: neuropsycholinguistic abilities and imaging analysis of the central nervous system
(Assoc Arquivos Neuro- Psiquiatria, 2017-12-01)
Objective: To characterize patients with syndromic craniosynostosis with respect to their neuropsycholinguistic abilities and to present these findings together with the brain abnormalities. Methods: Eighteen patients with ...
Report of a father with congenital bilateral absence of the vas deferens fathering a child with beare–stevenson syndrome
(Frontiers In Genetics, 2023)
Apert syndrome: a case report in pediatric dentistrySíndrome de Apert. Reporte de caso en odontopediatría
(Universidad Nacional Mayor de San Marcos, Facultad de Odontología, 2011)
Técnica "H" de Renier para correção da escafocefalia descrição da primeira série de casos no Brasil
(Faculdade de Medicina da BahiaUFBAbrasil, 2015-11-19)
TECHNIQUE TO CORRECT SCAPHOCEPHALY: RENIER’S "H"
DESCRIPTION OF THE FIRST SERIES OF CASES IN BRAZIL. Background:
Craniosynostosis (CS) is the premature fusion of one or more cranial sutures leading to
deformities ...
Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspects
(2016-06-01)
Apert and Crouzon are the most common craniosynostosis syndromes associated with mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. We conducted a study to examine the molecular biology, brain abnormalities, ...
Cranio-oculo-fronto-nasal malformation: A new MCA condition?
(Chapman Hall LtdLondonInglaterra, 1997)