Cleft lip and cleft palate are two common but markedly different birth defects that affect about one in every 700 newborns. These developmental deformities occur in the first trimester of a woman’s pregnancy; cleft lip in week seven, and cleft palate in week nine. Cleft lip and cleft palate occur simultaneously in about half of all cases, and separately in approximately a quarter of all cases.
A cleft lip is essentially a separation of the two sides of the lip. In many cases, this separation will include the bone and gum of the upper jaw. A cleft palate occurs when the sides of the palate fail to “fuse” as the fetus is developing, which results in an opening in the roof of the mouth.
The cleft deformities are categorized according to their location in the mouth and the size of the defect.
A cleft on only one side of the mouth that does not extend as far as the nostril.
A cleft on only one side of the mouth that extends into the corresponding nostril.
Larger clefts affecting both sides of the mouth which each extend as far as the nostril.
A mild case of cleft lip which may simply form a bump on the lip, or a small scar line extending toward the nostril.
Cleft lip and cleft palate are highly treatable deformities, though it may take a whole team of different specialists to fully treat the condition. The prognosis for sufferers who receive corrective treatment is excellent; medically, physically, dentally, and emotionally. There are however, a series of risks for those who do not receive corrective treatment:
Children born with either cleft deformity are likely to experience speech problems unless treatment is sought. Speech problems are detrimental to a child’s social and emotional development.
Babies with a cleft palate or a complete cleft lip have problems drinking milk. The gap means that liquids can pass from the mouth to the nasal cavity. This can be dangerous unless the child is fed sitting upright.
A cleft palate can cause the eustachian tubes (connecting the throat to the ear) to be incorrectly positioned. The fluid build up which results from this poor positioning can lead to painful middle ear infections. Severe and prolonged ear infections can lead to complete hearing loss.
Abnormalities in the upper jaw, gum, or arch can cause teeth to become impacted (unable to erupt) or absent completely. The shape of the mouth might not permit proper brushing which can lead to periodontal disease and tooth decay.
Initially, surgeons will work to close the cleft openings in the first six months of the child’s life. Unfortunately, this does not cure the dental problems that occur as a result of cleft lip and cleft palate defects. A thorough examination of the teeth surrounding the deformity will be preformed.
The surgeon may need to graft the defect (gap) with bone and/or soft tissue. Dental implants may also be needed. These treatment will restore functionality to the upper jaw and improve the aesthetic appearance of the smile.
If your child was born with any cleft deformity, we strongly encourage you to contact our Katy oral surgery office to schedule a consultation with Houston oral surgeon John P. Freeman MD, DDS, FACS.