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Main genetic entities associated with supernumerary teeth.
Cammarata-Scalisi F, Avendaño A, Callea M. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2018 Dec 1;116(6):437-444. doi: 10.5546/aap.2018.eng.437. Arch Argent Pediatr. 2018. PMID: 30457727 Free article. Review. English, Spanish.
However, the presence of multiple impacted or erupted supernumerary teeth is rare and associated with some genetic syndromes: cleidocranial displasia, familial adenomatous polyposis, trichorhinophalangeal syndrome type I, Rubinstein-Taybi syndrome, Nance-Horan syndrome, Opitz G/B …
However, the presence of multiple impacted or erupted supernumerary teeth is rare and associated with some genetic syndromes: cleidocranial …
Oculofaciocardiodental syndrome: a rare case and review of the literature.
Davoody A, Chen IP, Nanda R, Uribe F, Reichenberger EJ. Davoody A, et al. Cleft Palate Craniofac J. 2012 Sep;49(5):e55-60. doi: 10.1597/10-256. Epub 2011 Jul 8. Cleft Palate Craniofac J. 2012. PMID: 21740180 Free PMC article. Review.
Oculofaciocardiodental syndrome is a rare genetic disorder affecting ocular, facial, dental, and cardiac systems. The clinical diagnosis of oculofaciocardiodental syndrome can be challenging due to a wide variety of symptoms. ...
Oculofaciocardiodental syndrome is a rare genetic disorder affecting ocular, facial, dental, and cardiac systems. The clinical
Syndromes with supernumerary teeth.
Lubinsky M, Kantaputra PN. Lubinsky M, et al. Am J Med Genet A. 2016 Oct;170(10):2611-6. doi: 10.1002/ajmg.a.37763. Epub 2016 Jun 2. Am J Med Genet A. 2016. PMID: 27250821 Review.
We found only eight genetic syndromes with strong evidence for an association: cleidocranial dysplasia; familial adenomatous polyposis; trichorhinophalangeal syndrome, type I; Rubinstein-Taybi syndrome; Nance-Horan syndrome; Opitz BBB/G syndrome; oculofaciocardiodental
We found only eight genetic syndromes with strong evidence for an association: cleidocranial dysplasia; familial adenomatous polyposis; tric …
Eye development genes and known syndromes.
Slavotinek AM. Slavotinek AM. Mol Genet Metab. 2011 Dec;104(4):448-56. doi: 10.1016/j.ymgme.2011.09.029. Epub 2011 Sep 29. Mol Genet Metab. 2011. PMID: 22005280 Free PMC article. Review.
This review provides clinical and molecular information for several of the commonest syndromes associated with A/M: Anophthalmia-Esophageal-Genital syndrome, caused by SOX2 mutations, Anophthalmia and pituitary abnormalities caused by OTX2 mutations, Matthew-Wood syndrome caused …
This review provides clinical and molecular information for several of the commonest syndromes associated with A/M: Anophthalmia-Esophageal- …