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 8
1989 9
1990 11
1991 14
1992 12
1993 14
1994 11
1995 18
1996 18
1997 22
1998 13
1999 5
2000 14
2001 18
2002 9
2003 9
2004 11
2005 11
2006 15
2007 12
2008 11
2009 5
2010 10
2011 14
2012 14
2013 14
2014 25
2015 21
2016 15
2017 13
2018 13
2019 20
2020 13
2021 17
2022 15
2023 15
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

530 results

Results by year

Filters applied: . Clear all
Page 1
Treacher Collins Syndrome.
Aljerian A, Gilardino MS. Aljerian A, et al. Clin Plast Surg. 2019 Apr;46(2):197-205. doi: 10.1016/j.cps.2018.11.005. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851751 Review.
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displays an intricate underlying dysmorphology. ...Standard craniofacial procedures for bony and soft tissue reconstruction are used. ...
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displ …
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.
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 syndrome, and …
Clinicians use different diagnostic terms for patients with underdevelopment of facial features arising from the embryonic first and second …
Freeman-Burian syndrome.
Poling MI, Dufresne CR, Chamberlain RL. Poling MI, et al. Orphanet J Rare Dis. 2019 Jan 10;14(1):14. doi: 10.1186/s13023-018-0984-2. Orphanet J Rare Dis. 2019. PMID: 30630514 Free PMC article. Review.
CLINICAL DESCRIPTION: Freeman-Burian syndrome (FBS) is a rare congenital myopathic craniofacial syndrome. Considerable variability in severity is seen, but diagnosis requires the following: microstomia, whistling-face appearance (pursed lips), H or V-shaped chin defect, an …
CLINICAL DESCRIPTION: Freeman-Burian syndrome (FBS) is a rare congenital myopathic craniofacial syndrome. Considerable variability in …
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.
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 …
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. Patients …
Anatomic studies have identified that patients with Treacher Collins syndrome and some cases of bilateral craniofacial microsomia are …
Craniofacial Microsomia.
Brandstetter KA, Patel KG. Brandstetter KA, et al. Facial Plast Surg Clin North Am. 2016 Nov;24(4):495-515. doi: 10.1016/j.fsc.2016.06.006. Facial Plast Surg Clin North Am. 2016. PMID: 27712817 Review.
Craniofacial microsomia (CFM) encompasses a broad spectrum of phenotypes. ...
Craniofacial microsomia (CFM) encompasses a broad spectrum of phenotypes. ...
530 results