Results 151 to 160 of about 12,911 (203)
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Facial Clefts and Facial Dysplasia

Journal of Craniofacial Surgery, 2014
Most craniofacial malformations are identified by their appearance. The majority of the classification systems are mainly clinical or anatomical, not related to the different levels of development of the malformation, and underlying pathology is usually not taken into consideration.
Riccardo F, Mazzola, Isabella C, Mazzola
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Oblique Facial Clefts

Scandinavian Journal of Plastic and Reconstructive Surgery, 1980
In a material of about 3600 facial clefts eleven oblique clefts were observed (3.1%o). The most frequent types were the medial oro-ocular and naso-ocular clefts and their combinations. There were two atypical cases and one lateral oro-ocular variety. The oblique clefts were frequently associated with other types of clefts and/or more distant anomalies.
A. Rintala   +3 more
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Facial Cleft No. 1

Plastic and Reconstructive Surgery, 1994
The anomaly of facial cleft no. 1 has been encountered recently. It is a rare finding and, accordingly, is being reported with the hope that more craniofacial clefts will be seen in the future and direct the attention of the medical community to the problems.
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Facial Clefts Among Epileptic Patients

Archives of Neurology, 1981
Anticonvulsants have been suspected of teratogenicity, with facial clefts being the malformation most frequently associated with maternal anticonvulsant therapy. Paternal epilepsy has also been suggested as a factor in the genesis of birth defects, including facial clefts. An association between epilepsy per se and facial clefts would be reflected in a
M L, Fris   +5 more
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Oblique Facial Clefts

Plastic and Reconstructive Surgery, 1985
Modern views on embryology have increased our understanding of the nature of oblique facial clefts. The anomalies that have their origin at the junction of facial processes, such as the nasomaxillary dysplasias, may be named primary clefts or transformation.
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LATERAL FACIAL CLEFTS

Plastic and Reconstructive Surgery, 1950
H M, BLACKFIELD, N J, WILDE
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[Unusual facial clefts].

Annales de chirurgie plastique et esthetique, 1999
After briefly review facial morphogenesis, the authors define facial clefts, distinguishing primary clefts, secondary clefts, and residual clefts. They discuss the uncertainties surrounding the embryology and clinical features of palpebral colobomas. The various pathogenetic concepts are analysed: amniotic hypothesis, vascular hypothesis, fusion defect.
M, Stricker   +5 more
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Bilateral complete transverse facial cleft

Journal of Pediatric Surgery, 1980
A rare case of bilateral complete transverse cleft in an otherwise normal newborn male baby is presented. The operative management and the technique of repair adopted by the author are described. The result proves that the technique of operation by mucosal flaps as described here gives a good cosmetic appearance.
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Facial Cleft in a Newborn

Indian Journal of Otolaryngology and Head & Neck Surgery
A term newborn was detected for a rare facial defect in the delivery room. The defect arose due to malunion along the lines of facial development during fetal life. This embryonic defect is classified according to the areas of face involved and its associated structures.
Ankita Mandal, Chetan Khare
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Median Facial Cleft With Hypotelorism

Archives of Pediatrics & Adolescent Medicine, 1968
THE central part of the face and the forebrain are closely connected in early development, and when midline facial defects occur, there is often concomitant maldevelopment of the anterior part of the brain.1It was at first thought that the cerebral anomaly consisted of a lack of development of the olfactory bulb, tract, and cortex (arhinencephaly); but
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