“Cleft lip and cleft palate” are congenital conditions characterized by openings or splits in the upper lip, the roof of the mouth (palate), or both. These occur when the facial structures of an unborn baby fail to fully fuse during development.
These conditions are among the most prevalent birth defects, often presenting as isolated anomalies but may also be associated with various inherited genetic conditions or syndromes.
While the birth of a baby with a cleft can be distressing, both cleft lip and cleft palate can be effectively corrected. A series of surgeries in infancy and childhood can restore normal function and achieve a more typical appearance with minimal scarring in most cases.
Classification
Cleft lip and palate repairs are categorized based on several factors, including the severity of the cleft and the specific technique used for correction. The classifications commonly used include:
- Primary Repair: It involves the first surgical procedure aimed at closing the cleft lip or palate. This procedure is typically performed during infancy, usually between 2 to 6 months of age for cleft lip and between 6 to 18 months for cleft palate.
- Unilateral vs. Bilateral: Clefts may be as unilateral, affecting one side, or bilateral, affecting both sides, of the lip and/or palate. The surgical approach is tailored accordingly based on the specific type of cleft.
- Complete versus incomplete classification: It pertains to the extent of the cleft. A complete cleft signifies a full separation of the lip or palate tissues, whereas an incomplete cleft denotes partial separation.
- Primary vs. Secondary Repair: It denotes the initial surgical closure of the cleft, while secondary repair involves subsequent procedures performed to address residual issues or enhance aesthetic outcomes as the child matures.
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