cleft palate


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cleft

 [kleft]
1. a fissure or longitudinal opening, especially one occurring during embryonic development.
2. having such a fissure.
branchial cleft
1. one of the slitlike openings in the gills of fish between the branchial arches.
facial cleft
1. any of the clefts between the embryonic prominences that normally unite to form the face.
2. failure of union of one of these embryonic clefts; depending on the site, this causes such developmental defects as cleft cheek, cleft mandible, or cleft lip. Called also prosoposchisis.
cleft lip (cleft palate) congenital fissure, or split, of the lip (cleft lip) or of the roof of the mouth (cleft palate); one or the other occurs in about one birth per thousand. Sometimes they are associated with clubfoot (talipes) or other anatomic defects. They have no connection with mental retardation. Although poor health of the mother during pregnancy may have some effect on the development of her child, the old superstition that psychologic experiences of the pregnant mother can cause cleft palate and cleft lip has no scientific basis. However, it is true that parents who were born with cleft palate or cleft lip are somewhat more likely than other parents to have children with these defects.

Cleft palate and cleft lip result from failure of the two sides of the face to unite properly at an early stage of prenatal development. The defect may be limited to the outer flesh of the upper lip (the term harelip, suggesting the lip of a rabbit, is both inaccurate and unkind), or it may extend back through the midline of the upper jaw through the roof of the palate. Sometimes only the soft palate, located at the rear of the mouth, is involved.

The infant with a cleft palate is unable to suckle properly, because the opening between mouth and nose through the palate prevents suction. Feeding must be done by other means, with a dropper, a cup, a spoon, or an obturator, a device inserted in the mouth to close the cleft while the baby is sucking. Cleft palate allows food to get into the nose, and it causes difficulty in chewing and swallowing. Later it will hinder speech, because consonants such as g, b, d, and f, which are normally formed by pressure against the roof of the mouth, are distorted by resonance in the nasal cavity. The cleft may also prevent movements of the soft palate essential in clear speech.
Treatment. Treatment of cleft palate and cleft lip is by surgery, followed by measures to improve speech. A cleft palate should be reconstructed by plastic surgery when the child is about 18 months old, before he learns to talk. The corrective work usually requires only one operation. After surgery, the child often needs special training in speech to facilitate communication and maintain self-esteem. Cleft lip usually can be corrected by surgery when the child reaches a weight of 12 to 15 lb (5.4 to 7 kg), generally at the age of 2 to 3 months. Successful surgery often leaves only a thin scar and a greatly improved ability to form the p, b, and m sounds. A child born with a moderate degree of cleft palate or cleft lip can look forward to a life normal in appearance, speech, and manner if proper action is taken early. This means consulting and carefully following the advice of competent specialists in medicine, surgery, dentistry, and speech.
Patient Care. The main concerns during the preoperative period are maintenance of adequate nutrition, prevention of respiratory infections, and speech therapy to prevent development of bad habits of speech. Postoperative care must be aimed at prevention of trauma to or infection of the operative site. The child is not allowed to lie prone until the incision is completely healed. Elbow restraints are used to keep the fingers and hands away from the mouth. The patient is usually fed with a special syringe with a rubber tip as long as only liquids are allowed. When a soft diet is prescribed, care must be taken that the spoon or other eating utensils do not damage the suture line. Mouth care is given frequently to keep the mouth clean and reduce the danger of infection. Dental caries often occurs in patients with cleft palate and regular visits to the dentist are needed. Tender loving care, always a part of pediatric care, is even more necessary when caring for these children. They must be reassured and kept quiet so that crying and restlessness do not undo the work done by the surgeon. (See Atlas 1, Part A.)
A, Severe and B, mild form of cleft lip/palate. From Mueller et al., 2001.

palate

 [pal´at]
the roof of the mouth. The hard palate is the front portion braced by the upper jaw bones (maxillae); it has a bony framework and forms the partition between the mouth and the nose. The soft palate is the fleshy part arching downward from the hard palate to the throat; it separates the mouth and the pharynx. When a person swallows, the rear of the soft palate swings up against the back of the pharynx and blocks the passage of food and air to the nose. A fleshy lobe called the uvula hangs from the middle of the soft palate. adj., adj pal´atal.
cleft palate see cleft lip and cleft palate.
premaxillary palate (primary palate) that portion of the palate that was the median nasal process during early development.
secondary palate that portion of the palate that was the lateral nasal processes during early development.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.

cleft pal·ate

a congenital fissure in the median line of the palate, often, but not necessarily associated with cleft lip. May occur as a component of other craniofacial anomalies or other syndromes, for example, diastrophic dwarfism or spondyloepiphysial dysplasia congenita; its general genetic incidence resembles that of cleft lip (1 in 750-1000 live births).
Farlex Partner Medical Dictionary © Farlex 2012

cleft palate

n.
A congenital fissure in the roof of the mouth, resulting from incomplete fusion of the palate during embryonic development. It may involve only the uvula or extend through the entire palate.
The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.

cleft palate

Embryology A congenital defect characterized by a failure in the fusion of the hard and/or soft palate, often associated with cleft lip. See Cleft lip.
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.

cleft pal·ate

(kleft pal'ăt)
A congenital fissure in the median line of the palate, often associated with cleft lip; often occurs as a feature of a syndrome or generalized condition (e.g., diastrophic dwarfism or spondyloepiphysial dysplasia congenita); its general genetic behavior resembles that of cleft lip
Synonym(s): palatoschisis.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012

Cleft palate

A congenital malformation in which there is an abnormal opening in the roof of the mouth that allows the nasal passages and the mouth to be improperly connected.
Gale Encyclopedia of Medicine. Copyright 2008 The Gale Group, Inc. All rights reserved.

cleft pal·ate

(kleft pal'ăt)
Congenital fissure in median line of the palate, often, but not necessarily associated with cleft lip.
Medical Dictionary for the Dental Professions © Farlex 2012
References in periodicals archive ?
Universal parameters for reporting speech outcomesin individuals with cleft palate. Cleft Palate Craniofac J.
Exposure to certain substances during pregnancy: Cleft lip and cleft palate may be more likely to occur in pregnant women who smoke cigarettes, drink alcohol or take certain medications .
Inheritance of harelip and cleft palate. Copenhagen: Arnold Busck 1942.
Prevalence, pattern and perceptions of cleft lip and cleft palate among children born in two hospitals in Kisoro District, Uganda.
Effects of having a cleft lip or cleft palate include difficulty in feeding and speaking, but the largest effect remains to be emotional, with children suffering from bullying and low self-esteem because of their appearance.
Feeding obturator or appliance in a cleft palate patient: A case report.
The primary criticism of both our and previous synthetic cleft palate bench models [sup][1],[2],[3],[4],[5] has been their lack of fidelity with actual surgical practice.
Cleft palate is an opening between the mouth (oral cavity) and the nose (nasal cavity) that occurs when the tissues separating these two cavities do not grow together properly and it is a congenital disease.
Most of the recent literature recommends repair of cleft palate between 6 months to 18 months for best possible speech development and midfacial growth4.
ISLAMABAD -- Islamabad Cleft Lip and Plate Association (ICLAPA), which carried out free operations of cleft lip or cleft palate kinds, has decided to build a specialized hospital for the general treatment of children along with post-care health facilities.
Background: Cleft lip with or without cleft palate (CL/P) is one of the most common congenital anomalies and the etiology of orofacial clefts is multifactorial.
The authors do believe that more support is needed for young adults with a cleft palate condition after they reach the age of 18, especially when they are deciding to start families; they should be fully informed of the hereditary impact of their condition.