Results 301 to 310 of about 72,997 (336)
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The Lancet, 2009
Clefts of the lip and palate are generally divided into two groups, isolated cleft palate and cleft lip with or without cleft palate, representing a heterogeneous group of disorders affecting the lips and oral cavity. These defects arise in about 1.7 per 1000 liveborn babies, with ethnic and geographic variation. Effects on speech, hearing, appearance,
Mossey, Peter A. +4 more
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Clefts of the lip and palate are generally divided into two groups, isolated cleft palate and cleft lip with or without cleft palate, representing a heterogeneous group of disorders affecting the lips and oral cavity. These defects arise in about 1.7 per 1000 liveborn babies, with ethnic and geographic variation. Effects on speech, hearing, appearance,
Mossey, Peter A. +4 more
openaire +3 more sources
Clinics in Perinatology, 2018
Orofacial clefts are common congenital malformations with genetic and environmental risk factors. In the perinatal period, feeding and nutrition can be a challenge and the need for specialized feeders is common. Lip taping and nasoalveolar molding are early interventions that can be used to preoperatively modify cleft defects to enhance surgical ...
Mitchell L, Worley +2 more
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Orofacial clefts are common congenital malformations with genetic and environmental risk factors. In the perinatal period, feeding and nutrition can be a challenge and the need for specialized feeders is common. Lip taping and nasoalveolar molding are early interventions that can be used to preoperatively modify cleft defects to enhance surgical ...
Mitchell L, Worley +2 more
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Otolaryngologic Clinics of North America, 2000
The most common congenital deformity of the head and neck, cleft lip and palate, presents the surgeon with a unique esthetic and reconstructive challenge. The complexity of these deformities demands the skills of a multidisciplinary team of professionals to optimize surgical outcome.
R E, Kirschner, D, LaRossa
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The most common congenital deformity of the head and neck, cleft lip and palate, presents the surgeon with a unique esthetic and reconstructive challenge. The complexity of these deformities demands the skills of a multidisciplinary team of professionals to optimize surgical outcome.
R E, Kirschner, D, LaRossa
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Australian Dental Journal, 1973
Please refer to the ‘Instructions for Preparation of Specific Manuscript Categories’. Footnotes: Avoid footnotes. When essential, they are numbered consecutively and typed at the foot of the appropriate page. Tables and Illustrations: Tables and illustrations (both numbered in Arabic numerals) should be prepared on separate sheets.
W F, Brogan, H, McComb
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Please refer to the ‘Instructions for Preparation of Specific Manuscript Categories’. Footnotes: Avoid footnotes. When essential, they are numbered consecutively and typed at the foot of the appropriate page. Tables and Illustrations: Tables and illustrations (both numbered in Arabic numerals) should be prepared on separate sheets.
W F, Brogan, H, McComb
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Infants with Cleft Lip/Cleft Palate
Pediatrics In Review, 1988A cleft of the lip and/or palate occurs approximately once in 750 live births with some variability among various racial groups. As an isolated defect, cleft lip with or without cleft palate is etiologically distinct from cleft palate alone. More than 250 clefting syndromes, most of them relatively uncommon, have been described.
L, Suslak, F, Desposito
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The Embryology of Cleft Lip and Cleft Palate
Clinics in Plastic Surgery, 1975During recent years, rapid progress has been made in research related to normal embryonic facial development and the alterations which lead to the formation of clefts of the lip and palate. Characteristic developmental alterations of both genetic and environmental origin lead to different kinds of facial clefts.
M C, Johnston, J R, Hassell, K S, Brown
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Otolaryngologic Clinics of North America, 2007
Patients who have cleft lip or palate face significant lifelong communicative and aesthetic challenges and difficulties with deglutition. Management of patients who have orofacial clefting requires an understanding of the anatomy and pathophysiology associated with clefting and the developmental difficulties encountered by these patients.
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Patients who have cleft lip or palate face significant lifelong communicative and aesthetic challenges and difficulties with deglutition. Management of patients who have orofacial clefting requires an understanding of the anatomy and pathophysiology associated with clefting and the developmental difficulties encountered by these patients.
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Plastic Surgical Nursing, 1992
Families of infants born with congenital defects such as cleft lip, cleft palate, and combinations of these often grasp with accepting the condition. Nurses can help facilitate acceptance by parents and families and play a key role in the management and habilitation of these children.
S W, Wirt, C L, Algren, S L, Arnold
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Families of infants born with congenital defects such as cleft lip, cleft palate, and combinations of these often grasp with accepting the condition. Nurses can help facilitate acceptance by parents and families and play a key role in the management and habilitation of these children.
S W, Wirt, C L, Algren, S L, Arnold
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Journal of Craniofacial Surgery, 2017
Introduction: Cleft lip and palate is the most frequent congenital craniofacial deformity. In this article, the authors describe their experience with cleft lip and palate repair. Methods: Data regarding patients presenting with primary diagnosis of cleft lip and/or palate, between ...
Gian Luca, Gatti +4 more
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Introduction: Cleft lip and palate is the most frequent congenital craniofacial deformity. In this article, the authors describe their experience with cleft lip and palate repair. Methods: Data regarding patients presenting with primary diagnosis of cleft lip and/or palate, between ...
Gian Luca, Gatti +4 more
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Clefts of the lip and palate in twins
British Journal of Plastic Surgery, 1972Summary The incidence of twins affected by cleft lip and palate deformity, in an unselected series over a 10-year period is reported. The case histories of five monozygotic twin pairs are recorded and certain features of the early maxillary growth in one twin pair are analysed, and the reasons for the differences found are discussed.
G B, Blake, G, Wreakes
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