Cleft Palate: From 2 Different Sources
A ?ssure in the roof of the mouth (palate) and/ or the lip which is present at birth. It is found in varying degrees of severity in about one in 700 children. Modern plastic surgery can greatly improve the functioning of lips and palate and the appearance of the baby. Further cosmetic surgery later may not be necessary. The parent of the child who has cleft lip and/ or palate will be given detailed advice speci?c to his or her case. In general the team of specialists involved are the paediatrician, plastic surgeon, dentist or orthodontic specialist, and speech therapist. (See PALATE, MALFORMATIONS OF.)
a fissure in the midline of the palate due to failure of the two sides to fuse in embryonic development. Only part of the palate may be affected, or the cleft may extend the full length with bilateral clefts at the front of the maxilla; it may be accompanied by a *cleft lip and disturbance of tooth formation. Cleft palates can be corrected by surgery.
The partition between the cavity of the mouth, below, and that of the nose, above. It consists of the hard palate towards the front, which is composed of a bony plate covered below by the mucous membrane of the mouth, above by that of the nose; and of the soft palate further back, in which a muscular layer, composed of nine small muscles, is similarly covered. The hard palate extends a little further back than the wisdom teeth, and is formed by the maxillary and palate bones. The soft palate is concave towards the mouth and convex towards the nose, and it ends behind in a free border, at the centre of which is the prolongation known as the uvula. When food or air is passing through the mouth, as in the acts of swallowing, coughing, or vomiting, the soft palate is drawn upwards so as to touch the back wall of the throat and shut o? the cavity of the nose. Movements of the soft palate, by changing the shape of the mouth and nose cavities, are important in the production of speech.... palate
A rare congenital abnormality characterised by the absence of one or more toes and a deep central cleft that divides the foot into two. It is sometimes known as lobster foot, or lobster claw. It may be accompanied by other congenital defects, such as CLEFT HAND, absent permanent teeth, CLEFT PALATE (and/or lip), absence of the nails, and defects of the eye.... cleft foot
A rare congenital abnormality characterised by the absence of one or more ?ngers and a deep central cleft that divides the hand into two. It is sometimes known as lobster hand. It may be accompanied by other congenital defects, such as CLEFT FOOT, absent permanent teeth, CLEFT PALATE (and/or lip), absence of the nails and defects of the eye.... cleft hand
see pharyngeal cleft.... branchial cleft
(harelip) the congenital deformity of a cleft in the upper lip, on one or both sides of the midline. It occurs when the three blocks of embryonic tissue that go to form the upper lip fail to fuse and it is often associated with a *cleft palate. Medical name: cheiloschisis.... cleft lip
(branchial cleft, visceral cleft) any of the paired segmented clefts in each side of the throat of the early embryo that correspond to the gills of fish. Soon after they have formed they close to form the *pharyngeal pouches, except for the first cleft, which persists as the external auditory meatus.... pharyngeal cleft
see pharyngeal cleft.... visceral cleft