Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Congenital craniofacial abnormality"'
Publikováno v:
The Cleft Palate-Craniofacial Journal. 55:287-291
Cleft lip and palate (CLP) is the most common congenital craniofacial abnormality. Obstructive sleep apnea syndrome (OSAS) is a highly prevalent but underdiagnosed disease and is frequently associated with craniofacial anomalies. There are few studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa23d82136c3bbab2e9455ea91dcb361
https://doi.org/10.1177/1055665617726538
https://doi.org/10.1177/1055665617726538
Publikováno v:
The Anatomical Record. 300:1409-1419
Palate development is an important morphogenetic event in facial development, including the fusion of the lateral and medial nasal portions of the frontonasal process and maxilla. Derailments of any of these events may result in cleft palate, the mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7effda3644cadbe86eea2ec72bd16f80
https://doi.org/10.1002/ar.23597
https://doi.org/10.1002/ar.23597
Publikováno v:
Journal of Dentomaxillofacial Science, Vol 1, Iss 1 (2016)
Gnatoschisis is the most common congenital craniofacial abnormality patients with Cleft Lip and/or Palate (CL&/P). Gnatoschisis cases underwent gnatoplasty. Panoramic radiograph is one means to establish a diagnosis and treatment plan with two-dimens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6546cf8ba9ceceb0733ab5b2a8b1f1
http://jdmfs.org/index.php/jdmfs/article/view/162
http://jdmfs.org/index.php/jdmfs/article/view/162
Publikováno v:
International Journal of Dental Research. 5:167
Background: Cleft lip and palate is the most common major congenital craniofacial abnormality noted, which is 1 in 700 births. Although inheritance may play a role, cleft lip and palate is considered to be of multifactorial etiology, including chemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c92cea5e12fd218cc03877f6dcd084c
https://doi.org/10.14419/ijdr.v5i2.8040
https://doi.org/10.14419/ijdr.v5i2.8040