High-arched palate

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High-arched palate
Specialty Medical genetics

A high-arched palate (also termed high-vaulted palate) is where the palate is unusually high and narrow. It is usually a congenital developmental feature that results from the failure of the palatal shelves to fuse correctly in development, the same phenomenon that leads to cleft palate. [1] It may occur in isolation or in association with a number of conditions. It may also be an acquired condition caused by chronic thumb-sucking. A high-arched palate may result in a narrowed airway and sleep disordered breathing. [2]

Contents

Examples of conditions which may be associated with a high-arched palate include:

See also

Related Research Articles

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Pierre Robin sequence is a congenital defect observed in humans which is characterized by facial abnormalities. The three main features are micrognathia, which causes glossoptosis, which in turn causes breathing problems due to obstruction of the upper airway. A wide, U-shaped cleft palate is commonly also present. PRS is not merely a syndrome, but rather it is a sequence—a series of specific developmental malformations which can be attributed to a single cause.

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Sleep surgery is a surgery performed to treat sleep disordered breathing. Sleep disordered breathing is a spectrum of disorders that includes snoring, upper airway resistance syndrome, and obstructive sleep apnea. These surgeries are performed by surgeons trained in otolaryngology, oral maxillofacial surgery, and craniofacial surgery.

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<span class="mw-page-title-main">Bainbridge–Ropers syndrome</span> Human genetic disorder

Bainbridge–Ropers syndrome was first identified in 2013 and is characterized by failure to thrive, feeding problems, hypotonia, intellectual disabilities, autism, postnatal growth delay, abnormal facial features such as arched eyebrows, anteverted nares, and delays in language acquisition. BRPS is extremely rare worldwide; more than thirty cases of BRPS have been reported abroad, and four cases have been reported in China.

References

  1. Conley, Zachary R.; Hague, Molly; Kurosaka, Hiroshi; Dixon, Jill; Dixon, Michael J.; Trainor, Paul A. (15 July 2016). "A quantitative method for defining high-arched palate using the Tcof1(+/-) mutant mouse as a model". Developmental Biology. 415 (2): 296–305. doi:10.1016/j.ydbio.2015.12.020. ISSN   1095-564X. PMC   4914414 . PMID   26772999.
  2. Friedman M (2009). Sleep Apnea and Snoring: Surgical and Non-surgical Therapy. Elsevier Health Sciences. p. 6. ISBN   978-1-4160-3112-3.
  3. 1 2 Ghom AG; Ghom SA (1 July 2014). Textbook of Oral Medicine. JP Medical Ltd. pp. 810–812. ISBN   978-93-5152-303-1.
  4. Minić, S; Trpinac, D; Gabriel, H; Gencik, M; Obradović, M (January 2013). "Dental and oral anomalies in incontinentia pigmenti: a systematic review". Clinical Oral Investigations. 17 (1): 1–8. doi:10.1007/s00784-012-0721-5. PMC   3586138 . PMID   22453515.

Further reading