The skill of the surgeon, accurate presurgery markings, alignment of bones within the affected area, uncomplicated healing of the initial repair, and the effect of normal growth on the repaired lip.
Cleft lip has been documented throughout history, with evidence of surgical repair dating back to ancient times. The specific discovery of cleft lip as a congenital condition is not attributed to one individual, but rather has been recognized and treated by various civilizations over centuries.
Cleft lip occurs in approximately 1 in every 700 live births. It is one of the most common birth defects, affecting individuals of all ethnicities. The condition results from a combination of genetic and environmental factors.
A congenital fissure of the palate affecting the upper lip, hard palate, and soft palate is known as a cleft palate. This condition occurs during fetal development when the tissues forming the roof of the mouth do not fuse together properly. Cleft palate can lead to feeding difficulties, speech problems, and may require surgical intervention to repair.
Treatment for cleft lip typically involves surgery to repair the separation of the lip. The surgery is usually done in infancy to improve appearance and help with feeding and speech development. Follow-up care may include speech therapy and orthodontic treatment as the child grows.
Yes. He has a repaired cleft lip. His palate did not need repairing. His surgery took place when he was three months old
Cleft lip repair.
Cleft lip repair can be initiated at any age, but optimal results occur when the first operation is performed between two and six months of age. Surgery is usually scheduled during the third month of life.
Symmetrically shaped nostrils, and lips that appear as natural as possible and have a functional muscle.
Generally, cleft lip repair is well-tolerated in healthy infants. There are no major health problems associated with this reconstructive surgery.
The CPT Code fro palstic repair fo a bilateral cleft lip, primary bilateral in one stage is 40701. For unilateral without a stage, the CPT Code is 40700.
A cleft lip does not fuse properly during embryonic development. Surgical repair corrects the defect, preventing problems with breathing, speaking, eating, and improving physical appearance.
The skill of the surgeon, accurate presurgery markings, alignment of bones within the affected area, uncomplicated healing of the initial repair, and the effect of normal growth on the repaired lip.
Cleft lip is a congenital malformation in which the left and right sides of the upper lip do not join up properly. There may be genetic influences, as well as environmental or nutritional causes, but these are poorly understood. The proximate cause of cleft lip is a fusion defect, though.
A "cleft lip" affects just the patient's lip, and a "cleft palate" affects the palate, or the roof of your mouth.
Unilateral cleft lip results from failure of the maxillary prominence on the affected side to fuse with medial nasal prominences. The result is called a persistent labial groove.
Cupid's bow is a critical part of the repair, making it very important to accurately determine the high point of Cupid's bow on the lateral lip.
Cleft lip has been documented throughout history, with evidence of surgical repair dating back to ancient times. The specific discovery of cleft lip as a congenital condition is not attributed to one individual, but rather has been recognized and treated by various civilizations over centuries.