
A cleft is an abnormal vertical split or fissure between two body parts that should be joined together. It occurs during the development of the embryo. The palate is the upper and top portion of the mouth. It is the skeletal and muscular division that separates the nasal and oral cavities of the mouth. A cleft palate is a fissure in the roof of the mouth. It occurs when there is an abnormality of the two palatal shelves that ordinarily join together to form the complete palate. In some children, the front (hard) and back (soft) portions of the palate fail to join. In others, only one part of the palate is open.
A cleft lip is the presence of one or two abnormal, vertical splits in the upper lip. It can be a small opening or a sizable gap that goes from the lip to the nose. Cleft lip and palate are categorized as “orofacial” clefts because they affect the mouth and face. They are most common in babies of Asian and Native American descent.
There can be a cleft lip without cleft palate and vice versa, or both can occur simultaneously. This irregularity develops during pregnancy when there is insufficient tissue for the proper formation of the upper lip and palate, or when the tissue fails to join properly. Cleft lip and cleft palate can occur on both sides of the mouth as they develop separately. They affect the way the baby’s face looks and can lead to problems associated with eating, speaking, and listening.


