Abstract

Today, congenital cleft lip and palate (CCLP) is the most common congenital malformation of the maxillofacial area. According to different authors, the incidence of the defect among infants is 1 per 500--1000 depending on the region. In most cases, CCUPP is not difficult to diagnose; it is detected in the maternity hospital, and child with its parents is sent to a specialized institution for surgical treatment. However, there is a type of isolated cleft palate which may be very difficult to diagnose due to absence of evident defect of the palate. This is hidden (submucosal) congenital cleft palate. [1, 7].

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