Cleft palate In the
birth defect called
cleft palate, the left and right portions of this plate are not joined, forming a gap between the mouth and nasal passage (a related defect affecting the face is
cleft lip). While a cleft palate has a severe impact upon the ability to
nurse and speak, it is now successfully treated through reconstructive
surgical procedures at an early age. This is the time where such procedures are available. Due to the complexity of this birth defect, researchers still do not know exactly what causes the cleft palate to form during foetal development. Recently, these researchers found that even though there is no exact cause, there are several factors that drastically increase the risk of a baby being born with an orofacial cleft palate. As for the environmental risk factors, maternal smoking is the most influential risk factor. Based on a recent study of 103 German patients with cleft palates, it was found that 25.2% of their mothers smoked during pregnancy, a higher proportion than for the population as a whole. While maternal smoking during pregnancy is a risk, there are also several genetic risk factors. Six
single-nucleotide polymorphisms in the PAX7 gene are implicated in the development of facial features. Besides the PAX 7 gene variants, there were also five possible mutations found in the transforming growth factor-alpha gene (
TGFA) that could lead to the development of a cleft palate. Even though several risk factors have been linked to cleft palates, more research must be done in order to determine the true causes of the defect.
Palatal abscess Palatal
abscesses may also occur.
Hard palate pigmentation Long-term use of the drug
chloroquine diphosphatase, used in
malaria prophylaxis,
rheumatoid arthritis and other conditions, was found to cause bluish-grey pigmentation in the hard palate. ==See also==