Results 141 to 150 of about 12,911 (203)
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World Journal of Surgery, 1989
AbstractFacial clefts, including those of the lip and palate, are extremely rare. Some arise at the junction of facial processes preventing fusion, others have their origin in or between ossification centers. Virtually all are associated with osseous deficiencies.This article reviews the pathogenesis and morphology of these clefts.
J C, van der Meulen, J M, Vaandrager
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AbstractFacial clefts, including those of the lip and palate, are extremely rare. Some arise at the junction of facial processes preventing fusion, others have their origin in or between ossification centers. Virtually all are associated with osseous deficiencies.This article reviews the pathogenesis and morphology of these clefts.
J C, van der Meulen, J M, Vaandrager
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Polish Journal of Surgery, 2015
AbstractIn 1976 Dr. Paul Tessier described numeric classification for rare craniofacial clefts. He first emphasized that a fissure of the soft tissue corresponds, as a general rule, to a cleft of the bony structure. The classification, easy to understand, became widely accepted because the recording of the malformations was simple and facilitated ...
Marta, Fijałkowska +1 more
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AbstractIn 1976 Dr. Paul Tessier described numeric classification for rare craniofacial clefts. He first emphasized that a fissure of the soft tissue corresponds, as a general rule, to a cleft of the bony structure. The classification, easy to understand, became widely accepted because the recording of the malformations was simple and facilitated ...
Marta, Fijałkowska +1 more
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Archives of Otolaryngology - Head and Neck Surgery, 1981
Oblique facial clefts (meloschisis) are the most uncommon of the facial clefts, with 78 reports in the world literature. The embryology of this congenital deformity remains a matter of controversy. Details of surgical management are emphasized in the two reports of cases.
A T, Chiong, E S, Guevarra, R V, Zantua
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Oblique facial clefts (meloschisis) are the most uncommon of the facial clefts, with 78 reports in the world literature. The embryology of this congenital deformity remains a matter of controversy. Details of surgical management are emphasized in the two reports of cases.
A T, Chiong, E S, Guevarra, R V, Zantua
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Journal of Craniofacial Surgery, 1994
Midline clefts of the lower lip, mandible, tongue, and neck are rare congenital deformities and are classified as facial cleft no. 30 by Tessier. This is a report of a patient who presented with congenital fibrotic neck cord but no lower lip cleft, which has been the most frequently observed pathognomonic sign of this anomaly.
Keçeci Y. +3 more
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Midline clefts of the lower lip, mandible, tongue, and neck are rare congenital deformities and are classified as facial cleft no. 30 by Tessier. This is a report of a patient who presented with congenital fibrotic neck cord but no lower lip cleft, which has been the most frequently observed pathognomonic sign of this anomaly.
Keçeci Y. +3 more
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Lateral Facial Clefts (Macrostomia)
Annals of Plastic Surgery, 2001[Abstract Not Available]
Askar, I, Gurlek, A, Sevin, K
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Rare Facial Clefts. Cranifacial Anomalies
Plastic Surgical Nursing, 1998Craniofacial surgery is an integrated approach to correct anomalies that include a range of deformities in the growth of the cranium and facial bones. The goal of surgery is to achieve a maximum result with the best possible functional and aesthetic results with minimal scarring in the least amount of time.
C J, Parulski, B, Strohecker
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Bilateral Oblique Facial Cleft
Annals of Plastic Surgery, 1983An extremely rare case of bilateral oblique facial cleft is presented. This should be classified as a bilateral oroocular Type I cleft according to Boo-Chai's classification and a bilateral No. 4 cleft according to Tessier's classification. Except for this deformity, the patient was normal and healthy.
S, Sano, T, Tani, Y, Nishimura
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Scandinavian Journal of Plastic and Reconstructive Surgery, 1974
Within the compass of these few pages, we can only limn an abbreviated presentation of the subject of syndromes of facial clefting-as it were an antipasto to whet the appetite of the reader for further reading. Those of you who wish to seek expanded versions of this subject are referred to Gorlin, Cervenka & Pruzansky (1971) or especially to the ...
R J, Gorlin, J, Cervenka
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Within the compass of these few pages, we can only limn an abbreviated presentation of the subject of syndromes of facial clefting-as it were an antipasto to whet the appetite of the reader for further reading. Those of you who wish to seek expanded versions of this subject are referred to Gorlin, Cervenka & Pruzansky (1971) or especially to the ...
R J, Gorlin, J, Cervenka
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