Cleft Lip & Palate

OVERVIEW

Cleft Lip & Cleft Palate is a common birth condition. Cleft Lip & Cleft Palate are the result of tissues of the face not joining properly during development. As such, they are a type of birth defect. The cause is unknown in most cases. Risk factors include smoking during pregnancy, diabetes, obesity, an older mother, and certain medications (such as some used to treat seizures).

Cleft Lip & Cleft Palate can often be diagnosed during pregnancy with an ultrasound exam.

It can occur alone or as part of a genetic condition or syndrome.

Symptoms arise from the opening in the mouth. They include difficulty speaking and feeding.

Surgery restores normal function with minimal scarring. If required, speech therapy helps correct speaking difficulties.

SIGNS & SYMPTOMS

Cleft Lip & Cleft Palate, also known as orofacial cleft, is a group of conditions that includes cleft lip (CL), cleft palate (CP), and both together (CLP). A cleft lip contains an opening in the upper lip that may extend into the nose. The opening may be on one side, both sides, or in the middle. A cleft palate is when the roof of the mouth contains an opening into the nose. These disorders can result in feeding problems, speech problems, hearing problems, and frequent ear infections. Less than half the time the condition is associated with other disorders.