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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1988 2
1989 1
1990 3
1992 1
1995 1
1996 2
1998 1
1999 1
2000 1
2001 1
2002 1
2003 1
2008 2
2011 1
2012 1
2013 1
2014 2
2015 1
2016 1
2017 1
2018 1
2019 2
2020 1
2022 2
2023 1
2024 0

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32 results

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Page 1
Pai syndrome: a review.
Olivero F, Foiadelli T, Luzzi S, Marseglia GL, Savasta S. Olivero F, et al. Childs Nerv Syst. 2020 Nov;36(11):2635-2640. doi: 10.1007/s00381-020-04788-z. Epub 2020 Jul 10. Childs Nerv Syst. 2020. PMID: 32651596 Free PMC article. Review.
METHODS: We analyzed the PubMed database using the words "Pai syndrome", "frontonasal dysplasia", "cleft lip", "nasal polyp", "facial polyp", and "corpus callosum lipoma", including reviews, case reports and case series. ...
METHODS: We analyzed the PubMed database using the words "Pai syndrome", "frontonasal dysplasia", "cleft lip", "nasal polyp", …
Addressing hypertelorism: Indications and techniques.
Laure B, Batut C, Benouhagrem A, Joly A, Travers N, Listrat A, Pare A. Laure B, et al. Neurochirurgie. 2019 Nov;65(5):286-294. doi: 10.1016/j.neuchi.2019.09.007. Epub 2019 Sep 23. Neurochirurgie. 2019. PMID: 31557491 Review.
Oculoauriculovertebral spectrum: an updated critique.
Cohen MM Jr, Rollnick BR, Kaye CI. Cohen MM Jr, et al. Cleft Palate J. 1989 Oct;26(4):276-86. Cleft Palate J. 1989. PMID: 2680167 Review.
A number of conditions are discussed that are commonly differentiated from oculoauriculovertebral spectrum but have overlapping relationships, in some instances, with frontonasal dysplasia, branchio-oto-renal (BOR) syndrome, Townes-Brocks syndrome, Wildervanck syndr …
A number of conditions are discussed that are commonly differentiated from oculoauriculovertebral spectrum but have overlapping relationship …
Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review.
Serigatto HR, Kokitsu-Nakata NM, Vendramini-Pittoli S, Tonello C, Moura PP, Peixoto AP, Gomes LP, Zechi-Ceide RM. Serigatto HR, et al. Am J Med Genet A. 2023 Oct;191(10):2493-2507. doi: 10.1002/ajmg.a.63319. Epub 2023 Jun 7. Am J Med Genet A. 2023. PMID: 37282829 Review.
The oculoauriculofrontonasal syndrome (OAFNS) is a rare condition, with unknown etiology, characterized by the association of frontonasal dysplasia (FND) and oculoauriculovertebral spectrum (OAVS). ...
The oculoauriculofrontonasal syndrome (OAFNS) is a rare condition, with unknown etiology, characterized by the association of frontonasal
Marfan syndrome: from gene to therapy.
Bolar N, Van Laer L, Loeys BL. Bolar N, et al. Curr Opin Pediatr. 2012 Aug;24(4):498-504. doi: 10.1097/MOP.0b013e3283557d4c. Curr Opin Pediatr. 2012. PMID: 22705998 Review.
Acromelic frontonasal dysostosis.
Slaney SF, Goodman FR, Eilers-Walsman BL, Hall BD, Williams DK, Young ID, Hayward RD, Jones BM, Christianson AL, Winter RM. Slaney SF, et al. Am J Med Genet. 1999 Mar 12;83(2):109-16. Am J Med Genet. 1999. PMID: 10190481 Review.
In contrast, the upper limbs were normal. This rare variant of frontonasal dysplasia may represent a distinct autosomal-recessive disorder. ...
In contrast, the upper limbs were normal. This rare variant of frontonasal dysplasia may represent a distinct autosomal-recess …
Frontonasal dysplasia: analysis of 21 cases and literature review.
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen MM Jr. Guion-Almeida ML, et al. Int J Oral Maxillofac Surg. 1996 Apr;25(2):91-7. doi: 10.1016/s0901-5027(96)80048-8. Int J Oral Maxillofac Surg. 1996. PMID: 8727576 Review.
Twenty-one patients with frontonasal dysplasia were studied. A 2:1 male-to-female sex ratio and increased paternal and maternal ages at the time of conception were found. ...Three patients had the combination of agenesis of the corpus callosum, mental deficiency, an …
Twenty-one patients with frontonasal dysplasia were studied. A 2:1 male-to-female sex ratio and increased paternal and materna …
Toward clinical and molecular dissection of frontonasal dysplasia with facial skin polyps: From Pai syndrome to differential diagnosis through a series of 27 patients.
Lehalle D, Bruel AL, Vitobello A, Denommé-Pichon AS, Duffourd Y, Assoum M, Amiel J, Baujat G, Bessieres B, Bigoni S, Burglen L, Captier G, Dard R, Edery P, Fortunato F, Geneviève D, Goldenberg A, Guibaud L, Héron D, Holder-Espinasse M, Lederer D, Lopez Grondona F, Grotto S, Marlin S, Nadeau G, Picard A, Rossi M, Roume J, Sanlaville D, Saugier-Veber P, Triau S, Valenzuela Palafoll MI, Vanlerberghe C, Van Maldergem L, Vezain M, Vincent-Delorme C, Zivi E, Thevenon J, Vabres P, Thauvin-Robinet C, Callier P, Faivre L. Lehalle D, et al. Am J Med Genet A. 2022 Jul;188(7):2036-2047. doi: 10.1002/ajmg.a.62739. Epub 2022 Apr 21. Am J Med Genet A. 2022. PMID: 35445792 Review.
32 results