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  2. Cleft lip and cleft palate - Wikipedia

    en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate

    Submucous cleft palate can also occur, which is a cleft of the soft palate with a split uvula, a furrow along the midline of the soft palate, and a notch in the back margin of the hard palate. [12] The diagnosis of submucous cleft palate often occurs late in children as a result of the nature of the cleft. [13]

  3. Oral and maxillofacial pathology - Wikipedia

    en.wikipedia.org/wiki/Oral_and_maxillofacial...

    Cleft lip and palate is one of the most common occurring multi-factorial congenital disorder occurring in 1 in 500–1000 live births in several forms. [ 8 ] [ 9 ] [ 10 ] The most common form is combined cleft lip and palate and it accounts for approximately 50% of cases, whereas isolated cleft lip concerns 20% of the patients.

  4. Frontonasal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Frontonasal_dysplasia

    Frontonasal dysplasia (FND) is a congenital malformation of the midface. [1] For the diagnosis of FND, a patient should present at least two of the following characteristics: hypertelorism (an increased distance between the eyes), a wide nasal root, vertical midline cleft of the nose and/or upper lip, cleft of the wings of the nose, malformed nasal tip, encephalocele (an opening of the skull ...

  5. Velopharyngeal inadequacy - Wikipedia

    en.wikipedia.org/wiki/Velopharyngeal_inadequacy

    A cleft palate is one of the most common causes of VPI. Cleft palate is an anatomical abnormality that occurs in utero and is present at birth. This malformation can affect the lip and palate, or the palate only. A cleft palate can affect the mobility of the velopharyngeal valve, thereby resulting in VPI. [citation needed]

  6. Maxillary hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Maxillary_hypoplasia

    Maxillary hypoplasia is the most common secondary deformity that results from cleft lip and cleft palate. Because of the subjective nature of the diagnosis, the incidence of maxillary hypoplasia in people with cleft lip and palate varies between 15-50%. It is estimated that 25-50% of these patients require surgical intervention. [7]

  7. Craniofacial cleft - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_cleft

    There are several options for treatment of mouth anomalies like Tessier cleft number 2-3-7 . These clefts are also seen in various syndromes like Treacher Collins syndrome and hemifacial microsomia, which makes the treatment much more complicated. In this case, treatment of mouth anomalies is a part of the treatment of the syndrome.

  8. Classification of cleft lip and cleft palate - Wikipedia

    en.wikipedia.org/wiki/Classification_of_cleft...

    In ICD-10-CM, cleft lip is encoded by Q36.0-Q36.9; cleft palate by Q35.7-Q35.9; and cleft lip with cleft palate by Q37.8-Q37.9. Because ICD-9-CM and ICD-10-CM systems are very generic and do not adequately convey the complexity of the various forms of CL/P, modifications to these coding systems were developed for use in epidemiologic ...

  9. Vomer flap surgery - Wikipedia

    en.wikipedia.org/wiki/Vomer_flap_surgery

    A study that compared the effects of vomerine flap closure of the hard palate at the time of lip repair with non-closure of the hard palate in subjects with a unilateral cleft lip and palate found that the decrease of alveolar arch gap width at palate repair (6 months) in the vomerine flap group was significantly more than the decrease observed ...

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