description
incomplete fusion of the palatal shelves, which may be complete or incomplete, unilateral or bilateral. incomplete forms generally affect the secondary palate, posterior to the incisive foramen, and often occur without clefting of the lip. complete palatal clefts usually affect the primary and secondary palate and involve the lip. clefting of the primary palate alone does occur and generally includes a cleft lip. submucous clefts are those defects of the hard and soft palate where a mucosal web bridges the segments. the most frequent form of cleft palate is the bifid uvula, which is found in 2% of the population. a complete unilateral cleft palate is the next most common. midline clefts of the soft palate, which may or may not include part of the posterior hard palate, occur quite frequently. it has been suggested that v-shaped clefts of the palate are malformations whilst u-shaped clefts are deformations resulting from interference with palate shelf closure by the tongue. these latter clefts are often associated with micrognathia in the robin sequence. the incidence of isolated cleft palate is 4 to 5 per 10,000, and shows no racial or ethnic variation, in contrast to cleft lip and palate. complete clefts of the secondary palate are twice as common in females, whilst clefts of the velum show the opposite sex predominance. it is reported that up to 50% of infants with an isolated cleft palate have other congenital anomalies. many syndromic associations are noted.