Non-Random Distribution of Human Orofacial Clefts in Ghana: Gene-Environment Interactions

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Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts.

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Prenatal detection of orofacial clefts

Orofacial clefts are one of the most common congenital anomalies. The incidence is approximately 1 : 500 to 1 : 550 births [1]. The group of orofacial anomalies is heterogeneous. It comprises “typical” orofacial clefts ((cleft lip (CL), cleft lip and cleft palate (CLP) and cleft palate only (CP)) and “atypical” clefts (median, transversal, oblique and other Tessier’s types of facial clefts)[1]....

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[Prenatal detection of orofacial clefts].

Orofacial clefts are one of the most common congenital anomalies. The incidence is approximately 1 : 500 to 1 : 550 births [1]. The group of orofacial anomalies is heterogeneous. It comprises “typical” orofacial clefts ((cleft lip (CL), cleft lip and cleft palate (CLP) and cleft palate only (CP)) and “atypical” clefts (median, transversal, oblique and other Tessier’s types of facial clefts)[1]....

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An assessment of orofacial clefts in Tanzania

BACKGROUND Clefts of the lip (CL), the palate (CP), or both (CLP) are the most common orofacial congenital malformations found among live births, accounting for 65% of all head and neck anomalies. The frequency and pattern of orofacial clefts in different parts of the world and among different human groups varies widely. Generally, populations of Asian or Native American origin have the highest...

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ژورنال

عنوان ژورنال: Open Journal of Stomatology

سال: 2018

ISSN: 2160-8709,2160-8717

DOI: 10.4236/ojst.2018.82004