Cleft Palate and Cleft Lip: Defect in Infants

Cleft palate and cleft lip are one of the most common facial defects in infants. However, surgery can correct either one or both defects. Scientists are convinced that environmental and genetic factors can prevent the occurrence of cleft clefts or lips, but there is no concrete reason. Cleft palate is a palate cleft and may include a hard palate and / or soft palate.

Cleft lip and cleft is a birth defect in the face. Lip cleft affects the upper lip, from a notch to a complete crack extending from the nose. Palate cleavage affects the top of the mouth and has a groove extending through the arch. These exceptions may occur individually or together. Cleft lip and cleft cleft are face deformities that can occur alone or simultaneously. They may also be associated with other syndromes or birth defects. Lip separation can be completely separated from small notch to nose extension. The cause of these malformations may be mutated genes or teratogenic substances. Teratogenic substances are substances that cause abnormal fetal growth, such as certain viruses and chemicals. In addition to bad appearance, these abnormalities can also cause eating difficulties and speech development problems. Risk factors are the family history of cleft lip or cleft cleft and the presence of another congenital defect

I will split it. 22q 11.2 The common symptoms of deficiency syndrome are cleft clefts - openings above the mouth with or without cleft lip. Other less obvious sputum abnormalities that may be present may swallow or make it difficult to produce sounds in the speech. Unique facial features 22 q 11.2 Some people with a deletion syndrome may have many concrete facial features. These include small, low ears, short eye corners (eyelids), goggles, relatively long face, tip of nose (light bulb), or short or flat groove of upper lip.