"Mouth Abnormalities" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital absence of or defects in structures of the mouth.
| Descriptor ID |
D009056
|
| MeSH Number(s) |
C07.465.525 C07.650.525 C16.131.850.525
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Mouth Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Mouth Abnormalities".
This graph shows the total number of publications written about "Mouth Abnormalities" by people in this website by year, and whether "Mouth Abnormalities" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 1 | 2 |
| 2005 | 2 | 0 | 2 |
| 2010 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mouth Abnormalities" by people in Profiles.
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Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate. Cleft Palate Craniofac J. 2022 Apr; 59(4):417-426.
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Craniofacial phenotypes associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3606-3612.
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Syngnathia and obstructive apnea in a case of popliteal pterygium syndrome. Eur J Pediatr. 2014 Dec; 173(12):1741-4.
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Diagnosing ankyloglossia. J Hum Lact. 2013 Aug; 29(3):423.
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Teratogenic effects of antiepileptic drugs. Expert Rev Neurother. 2010 Jun; 10(6):943-59.
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Polymorphisms in DNA repair genes as risk factors for spina bifida and orofacial clefts. Am J Med Genet A. 2005 Jun 15; 135(3):268-73.
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Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts? Am J Med Genet A. 2005 Jun 15; 135(3):274-7.
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New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay. Am J Med Genet. 2001 Jun 01; 101(1):70-3.
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Identification of the gene for oral-facial-digital type I syndrome. Am J Hum Genet. 2001 Mar; 68(3):569-76.
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Limb anomalies following chorionic villus sampling: a registry based case-control study. Am J Med Genet. 1992 Dec 01; 44(6):856-64.