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The Cleft Palate-Craniofacial Journal is a monthly peer-reviewed medical journal. It was established in 1964 as the Cleft Palate Journal , obtaining its current title in 1991. [ 1 ] The journal is published by SAGE Publishing on behalf of the American Cleft Palate-Craniofacial Association .
The Cleft Palate-Craniofacial Journal: Craniofacial Medicine: SAGE Publishing: English: 1964–present Clinical Anatomy: Medicine: Wiley-Liss: English: 1988–present Clinical and Experimental Gastroenterology: Gastroenterology: Dove Medical Press: English: 2008–present Clinical and Translational Science: Medicine: Wiley-Blackwell: English ...
Cleft lip and palate is one of the most common occurring multi-factorial congenital disorder occurring in 1 in 500–1000 live births in several forms. [ 8 ] [ 9 ] [ 10 ] The most common form is combined cleft lip and palate and it accounts for approximately 50% of cases, whereas isolated cleft lip concerns 20% of the patients.
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The Nance Obturator, a New Fixed Obturator for Patients with Cleft Palate and Fistula. Journal of Prosthodontics,21(5):400–403. Kuehn, D.P., & Moller, K.T. (2000).Speech and Language Issues in the Cleft PalatePopulation: The State of the Art. The Cleft Palate-Craniofacial Journal, 37, 348–348.
Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.The three main features are micrognathia (abnormally small mandible), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due to obstruction of the upper airway.
Veau-IV cleft palate: A cleft of the velum (soft palate), extending in the midline through the secondary hard palate up to the incisive foramen and then bilaterally through the primary hard palate and alveolus on each side. The vomer (the bony part of the nasal septum) remains in the midline and is attached to the premaxilla.
Hearing loss with craniofacial syndromes is a common occurrence. Many of these multianomaly disorders involve structural malformations of the outer or middle ear , making a significant hearing loss highly likely.