Due to the unique anatomical and physiological variations of the airway of a child with cleft lip and palate, anesthesiologists may find it difficult to manage it properly. As a result, cleft lip and palate surgery in children will necessitate careful attention, detailed understanding, and practical application in anaesthetic preparation. While the majority of individuals have isolated CLP, a considerable percentage of them also have related abnormalities. Other issues with the formation of the branchial arch are the most noticeable (e.g. ear or upper airway defects). Anomalies of the heart, kidneys, and skeleton are among them. Associated anomalies could be part of a defined pattern, indicating which flaws to expect; the number of such disorders, including CLP, is growing by the day, ranging from the obvious, such as Trisomy 21, to the more subtle, such as Velocardiofacial Syndrome. Here we report anaesthetic management of a 13 old girl with congenital complete cleft of soft palate with kyphoscoliosis posted for surgical repair of soft palate under general anesthesia.
Keywords: Cleft palate, Kyphoscoliosis, anaesthetic management.