Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1963 2
1964 2
1965 1
1967 1
1968 3
1969 2
1971 2
1972 5
1973 3
1974 6
1975 6
1976 3
1977 3
1978 3
1979 3
1980 3
1981 5
1982 3
1983 1
1984 1
1985 7
1986 3
1987 3
1988 10
1989 9
1990 11
1991 14
1992 12
1993 14
1994 11
1995 21
1996 19
1997 26
1998 14
1999 7
2000 16
2001 19
2002 11
2003 10
2004 13
2005 13
2006 15
2007 13
2008 11
2009 5
2010 10
2011 15
2012 17
2013 14
2014 30
2015 22
2016 17
2017 17
2018 17
2019 25
2020 14
2021 19
2022 18
2023 18
2024 9

Text availability

Article attribute

Article type

Publication date

Search Results

587 results

Results by year

Filters applied: . Clear all
Page 1
Treacher Collins Syndrome: Genetics, Clinical Features and Management.
Marszałek-Kruk BA, Wójcicki P, Dowgierd K, Śmigiel R. Marszałek-Kruk BA, et al. Genes (Basel). 2021 Sep 9;12(9):1392. doi: 10.3390/genes12091392. Genes (Basel). 2021. PMID: 34573374 Free PMC article. Review.
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second pharyngeal arches, occurring during fetal development. ...TCS occurs in the general population at a frequency of 1 in 50,000 live births. Four subtypes of Treacher Collins …
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second pharyngeal arches, occurring duri …
Goldenhar syndrome: current perspectives.
Bogusiak K, Puch A, Arkuszewski P. Bogusiak K, et al. World J Pediatr. 2017 Oct;13(5):405-415. doi: 10.1007/s12519-017-0048-z. Epub 2017 Jun 15. World J Pediatr. 2017. PMID: 28623555 Review.
BACKGROUND: Progress in medical branches that has taken place since the first child with Goldenhare syndrome (GS) had been described in 1952 by Maurice Goldenhar, facilitated better understanding of this congenital defect. ...Ethiopathogenesis is multifactorial and depende …
BACKGROUND: Progress in medical branches that has taken place since the first child with Goldenhare syndrome (GS) had been described …
Oculo-auriculo-vertebral spectrum: new genes and literature review on a complex disease.
Tingaud-Sequeira A, Trimouille A, Sagardoy T, Lacombe D, Rooryck C. Tingaud-Sequeira A, et al. J Med Genet. 2022 May;59(5):417-427. doi: 10.1136/jmedgenet-2021-108219. Epub 2022 Feb 2. J Med Genet. 2022. PMID: 35110414 Review.
Oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome is due to an abnormal development of first and second branchial arches derivatives during embryogenesis and is characterised by hemifacial microsomia associated with auricular, ocular and vertebral malformation …
Oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome is due to an abnormal development of first and second branchial arches …
Craniofacial Microsomia.
Birgfeld C, Heike C. Birgfeld C, et al. Clin Plast Surg. 2019 Apr;46(2):207-221. doi: 10.1016/j.cps.2018.12.001. Clin Plast Surg. 2019. PMID: 30851752 Review.
Clinicians use different diagnostic terms for patients with underdevelopment of facial features arising from the embryonic first and second pharyngeal arches, including first and second branchial arch syndrome, otomandibular dysostosis, oculoauriculovertebral syn …
Clinicians use different diagnostic terms for patients with underdevelopment of facial features arising from the embryonic first and second …
Craniofacial characteristics in Crouzon's syndrome: A systematic review and meta-analysis.
Alam MK, Alfawzan AA, Abutayyem H, Kanwal B, Alswairki HJ, Verma S, Ganji KK, Munisekhar MS, Siddiqui AA, Fahim A. Alam MK, et al. Sci Prog. 2023 Jan-Mar;106(1):368504231156297. doi: 10.1177/00368504231156297. Sci Prog. 2023. PMID: 36803068 Free PMC article. Review.
The purpose of this meta-analysis was to strengthen the credibility of primary research results by combining open-source scientific material, namely a comparison of craniofacial features (Cfc) between Crouzon's syndrome (CS) patients and non-CS populations. . …
The purpose of this meta-analysis was to strengthen the credibility of primary research results by combining open-source scientific material …
Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology.
Rai R, Iwanaga J, Dupont G, Oskouian RJ, Loukas M, Oakes WJ, Tubbs RS. Rai R, et al. Childs Nerv Syst. 2019 Sep;35(9):1451-1455. doi: 10.1007/s00381-019-04244-7. Epub 2019 Jun 21. Childs Nerv Syst. 2019. PMID: 31222448 Review.
The syndrome has been divided into three clinical subtypes based on clinical findings. METHODS: This review will specifically examine the most severe type, Pfeiffer syndrome type 2, focusing on its genetics and molecular biology. CONCLUSION: This subtype of the s …
The syndrome has been divided into three clinical subtypes based on clinical findings. METHODS: This review will specifically examine …
Crouzon syndrome and the eye: An overview.
Bhattacharjee K, Rehman O, Venkatraman V, Kikkawa D, Bhattacharjee H, Gogoi R, Grewal AM, Bhattacharjee P. Bhattacharjee K, et al. Indian J Ophthalmol. 2022 Jul;70(7):2346-2354. doi: 10.4103/ijo.IJO_3207_21. Indian J Ophthalmol. 2022. PMID: 35791116 Free PMC article. Review.
The current literature review aims to evaluate the ocular findings and associated ophthalmic features in Crouzon syndrome. Craniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common …
The current literature review aims to evaluate the ocular findings and associated ophthalmic features in Crouzon syndrome. Cra …
Syndromic Craniosynostosis.
Wang JC, Nagy L, Demke JC. Wang JC, et al. Facial Plast Surg Clin North Am. 2016 Nov;24(4):531-543. doi: 10.1016/j.fsc.2016.06.008. Facial Plast Surg Clin North Am. 2016. PMID: 27712819 Review.
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and other associated abnormalities, such as carpal-pedal anomalies and cognitive function impairment. ...
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and …
State-of-the-Art Hypertelorism Management.
Shakir S, Hoppe IC, Taylor JA. Shakir S, et al. Clin Plast Surg. 2019 Apr;46(2):185-195. doi: 10.1016/j.cps.2018.11.004. Epub 2019 Jan 9. Clin Plast Surg. 2019. PMID: 30851750 Review.
Counterclockwise Craniofacial Distraction Osteogenesis.
Hopper RA, Wang HD, Mercan E, Kapadia H. Hopper RA, et al. Clin Plast Surg. 2021 Jul;48(3):445-454. doi: 10.1016/j.cps.2021.02.006. Epub 2021 May 5. Clin Plast Surg. 2021. PMID: 34051897 Review.
Anatomic studies have identified that patients with Treacher Collins syndrome and some cases of bilateral craniofacial microsomia are characterized by multilevel airway obstruction as a result of hypoplasia and clockwise rotation of the maxillomandibular complex. Pa …
Anatomic studies have identified that patients with Treacher Collins syndrome and some cases of bilateral craniofacial microso …
587 results