MOLECULAR GENETICS OF CLEFT LIP AND PALATE: A REVIEW

Authors

G.O. Oboli1, D.I. Chukwuma2, O.F. Fagbule2, E.O. Abe3 and A.O. Adisa1,3

Correspondents

Dr. EO Abe
Department of Oral Pathology
and Oral Medicine,
University College Hospital,
Ibadan, Nigeria.
Email: eoabe83@yahoo.co.uk

Affiliation of Authors

College of Medicine, University of Ibadan, Ibadan
Department of Periodontology and Community Dentistry, University College Hospital, Ibadan
Department of Oral Pathology and Oral Medicine, University College Hospital, Ibadan

INTRODUCTION

Cleft lip with or without cleft palate (CLP) is a common congenital disability. They exist either in combination with one or more other anomalies (syndromic cleft) or in isolation (non-syndromic cleft). Non-syndromic CL/P is more common as it is present in about 70% of cases, out of which 80% are sporadic, and 20% are familial.1 CLP which is commoner in males, occurs in 1 out of 300 to 2500 births, while isolated cleft palate (CP) which occurs more frequently in females, occurs in 1 out of 1500 births2.3. People with cleft lip and palate often require multidisciplinary care involving several surgical repairs commencing in the first year of life, orthodontic interventions for malocclusion, speech therapy, treatment of recurrent middle ear infections, and psychological interventions. These have been noted to contribute a significant burden to the patient, family, and society at large. Thus, an intense effort has been made to unravel its aetiology, which would be important in genetic counselling, risk prediction, and overall prevention of cleft lip and palate4

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