The document discusses cleft lip and palate, defining clefts as fissures from incomplete fusion during facial development, with prevalence rates noted between 1:700 to 1:1000 live births, showing a male predominance. It covers embryology, genetics, and various classifications of cleft types, along with associated syndromes and teratogens that can contribute to clefting. The evolution of surgical techniques and timing for cleft lip repair is examined, emphasizing the importance of patient readiness based on age and weight.