Congenital anomalies of the maxillofacial region should be corrected in early childhood. Most often, this refers to a condition commonly known as a cleft lip, but medically known as a congenital cleft lip.
This is a disorder of soft and bone tissue formation that occurs early in the fetus's development in the womb.
This pathology is a failure of tissue fusion of the upper lip, which can affect only the skin or extend to the muscle layer, the maxillary bone, and the nasal cavity.
A congenital cleft lip is a lip that has not fused properly. The peculiarity of this pathology is that the integrity of the orbicularis oris muscle is disrupted. Instead of forming a single ring that ensures lip closure, the muscle fibers attach to the base of the nose and the premaxillary bone. This leads to deformation of the entire midface, including a deviated septum and a change in the shape of the alae nasi.
The main factor is genetic predisposition. However, this congenital malformation can also be caused by pregnancy itself. If a woman has been frequently ill, has had a folate deficiency, or has been exposed to toxic substances or radiation, the risk of cleft sac in the child increases. In most cases, doctors attribute the combination of factors to a disruption in the development of the fetus's facial structures.
Before surgery, the type of defect must be determined. Surgeons divide clefts into the following types:
A common combination of cleft lip and palate requires staged and longer treatment.
This material is for informational purposes only and does not constitute a guide to action. Please remember that cleft lip treatment is an individualized process. Preparation for the procedure and the scope of the examination will be determined by your treating physician during an in-person consultation. Our clinic offers a customized cleft lip correction plan, support throughout all stages of recovery, and the participation of specialized specialists in treatment planning.
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When correction is required
The main goal of treatment is to restore the anatomical integrity and function of the maxillofacial system. Surgery is performed between 3 and 6 months of age, unless there are medical contraindications.
Main indications for surgery
Surgery is almost always necessary. This is not only a matter of aesthetics, but also of the child's quality of life. A cleft can disrupt feeding because the child is unable to create the necessary suction. Breathing is also affected, and speech may be impaired in the future.
A doctor's consultation is necessary if:
When is revision surgery necessary?
Primary cheiloplasty addresses the main issues, but revision surgery may be necessary in preschool or adolescence. The treatment plan for each stage is determined individually, based on the developmental dynamics of the facial skeleton.