Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Annette C Da Costa"'
Autor:
David J. Amor, Katherine Sanchez, Nicky Kilpatrick, Annette C Da Costa, Jessica O Boyce, Sheena Reilly, Angela T Morgan
Publikováno v:
International Journal of Language & Communication Disorders. 54:767-778
Background: Submucous cleft palate (SMCP) has a heterogeneous presentation and is often identified late or misdiagnosed. Diagnosis is prompted by speech, resonance or feeding symptoms associated with velopharyngeal insufficiency. However, the broader
Publikováno v:
International Journal of Language & Communication Disorders. 53:959-968
Background Research investigating language skills in school-aged children with non-syndromic cleft lip and/or palate is sparse. Past studies focus on younger populations, lack key comparisons to demographically matched control cohorts or explore lang
Autor:
Kati J. Buckingham, Angela T Morgan, Damien Lederer, Annette C Da Costa, Susan M. White, Joanne Fifer, Kate Pope, Michael J. Bamshad, Margaret J. McMillin, Valérie Benoit, Cristina Mei
Publikováno v:
American Journal of Medical Genetics Part A. 167:1483-1492
Speech and language deficits are commonly associated with Kabuki syndrome. Yet little is known regarding the specific symptomatology of these disorders, preventing use of targeted treatment programs. Here we detail speech and language in 16 individua
Publikováno v:
Developmental Neuropsychology. 39:159-186
Children with single-suture craniosynostosis (SSC) are increasingly considered to be at high risk of adverse neurodevelopmental outcomes. This systematic review aimed to synthesise and critically appraise the existing literature on the neurodevelopme
Publikováno v:
Developmental Neuroscience. 36:490-498
Nonsyndromic cleft lip and palate (NSCLP) encompasses a group of orofacial abnormalities. Emerging evidence has revealed the presence of structural brain abnormalities in affected individuals. Previous studies have performed structure-based volumetri
Publikováno v:
Journal of Craniofacial Surgery. 24:1225-1228
The objective of this study was to characterize the early neurodevelopmental profile of Australian infants with deformational plagiocephaly (DP). Twenty-one infants with a confirmed diagnosis of DP (mean age, 7.9 months; SD, 2.0 months) were assessed
Autor:
David K. Chong, Vicki Anderson, Patrick Lo, Andrew L. Greensmith, Anthony D. Holmes, Annette C Da Costa, John G. Meara, Alison Wray
Publikováno v:
Child's Nervous System. 29:985-995
Nonsyndromic craniosynostosis (NSC) are a group of congenital disorders sharing premature fusion of one or more of the cranial sutures that restricts and distorts growth of the skull and underlying brain. This study examined the neurodevelopmental se
Autor:
Jacquie Wrennall, John G. Meara, David K. Chong, Ravi Savarirayan, Anthony D. Holmes, Andrew L. Greensmith, Vicki Anderson, Annette C Da Costa
Publikováno v:
Child's Nervous System. 28:869-877
Single-suture craniosynostosis (SSC) is a congenital craniofacial disorder, in which premature fusion of one of the skull sutures restricts and distorts growth of the cranium and underlying brain. This disorder of prenatal onset occurs during a criti
Autor:
John G. Meara, Vicki Anderson, Ravi Savarirayan, Jacquie Wrennall, Izabela Walters, Annette C Da Costa
Publikováno v:
Plastic and Reconstructive Surgery. 118:175-181
Background Craniosynostosis, the premature fusion of the skull bones, is a congenital deformity that has functional and morphologic implications. Cranial vault reconstructive surgery is required to improve skull shape and increase intracranial volume
Autor:
Annette C Da Costa, Alan Tucker, Ravi Savarirayan, Nicole Gardiner, John G. Meara, Jacquie Wrennall, Izabela Walters, Vicki Anderson
Publikováno v:
Annals of Plastic Surgery. 54:450-455
Apert syndrome is characterized by craniosynostosis, central nervous system anomalies, midface hypoplasia, and syndactyly. Current research has focused on genetic and neurologic correlates. Cognitive assessment has been primarily limited to global in