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

Year Number of Results
1972 1
1975 1
1979 1
1980 1
1981 2
1983 1
1984 1
1985 2
1986 1
1989 3
1990 1
1991 1
1992 2
1993 1
1994 1
1996 1
1997 2
1998 4
1999 3
2000 3
2001 2
2002 2
2003 2
2004 2
2005 2
2006 3
2008 2
2009 4
2010 2
2011 8
2012 6
2013 10
2014 6
2015 9
2016 7
2017 8
2018 3
2019 3
2020 6
2021 5
2022 6
2023 4
2024 3

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128 results

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Page 1
Presence and development of strabismus in children with telecanthus, epicanthus and hypertelorism.
Mooss VS, Kavitha V, Ravishankar HN, Heralgi MM, Aafreen S. Mooss VS, et al. Indian J Ophthalmol. 2022 Oct;70(10):3618-3624. doi: 10.4103/ijo.IJO_776_22. Indian J Ophthalmol. 2022. PMID: 36190058 Free PMC article.
PURPOSE: To study the presence and development of strabismus in children with telecanthus, epicanthus, and hypertelorism. METHODS: This is a prospective, longitudinal, and observational study. Sixty children aged between 6 months and 18 years with telecanthus, epica …
PURPOSE: To study the presence and development of strabismus in children with telecanthus, epicanthus, and hypertelorism. METHODS: Th …
Sincipital encephaloceles.
Singh AK, Upadhyaya DN. Singh AK, et al. J Craniofac Surg. 2009 Sep;20 Suppl 2:1851-5. doi: 10.1097/SCS.0b013e3181b6c49a. J Craniofac Surg. 2009. PMID: 19816364
Correction of encephaloceles can be done in 1 stage or multiple stages and consists of excision of the encephalocele sac, repair of the bony defect, correction of hypertelorism/telecanthus, and correction of associated deformities such as trigonocephaly and the "long nose. …
Correction of encephaloceles can be done in 1 stage or multiple stages and consists of excision of the encephalocele sac, repair of the bony …
Proboscis Lateralis With Choanal Atresia.
Gómez Prada DC, Restrepo Salamanca N, Sosa Castro OM. Gómez Prada DC, et al. J Craniofac Surg. 2024 Jan-Feb 01;35(1):211-214. doi: 10.1097/SCS.0000000000009869. Epub 2023 Nov 20. J Craniofac Surg. 2024. PMID: 37983369 Review.
The case of a female patient who was born with proboscis lateralis, choanal atresia, and telecanthus is submitted. A report is made on the initial management of this patient, the clinical follow-up that has been carried out so far, and a review of the literature is conduct …
The case of a female patient who was born with proboscis lateralis, choanal atresia, and telecanthus is submitted. A report is made o …
The Arrhinias.
Tessier P, Ciminello FS, Wolfe SA. Tessier P, et al. Scand J Plast Reconstr Surg Hand Surg. 2009;43(4):177-96. doi: 10.1080/02844310802517259. Scand J Plast Reconstr Surg Hand Surg. 2009. PMID: 19401938
The anomalies common to the three groups of Arrhinias are many: the agenesis of the nasal bones, the telecanthus which is often in contrast to the hypo-telorbitism, the obstruction of the naso-lacrimal passage, the ectasia of the lacrimal sac with an erosion of the inferom …
The anomalies common to the three groups of Arrhinias are many: the agenesis of the nasal bones, the telecanthus which is often in co …
Naso-ethmoid-orbital fractures.
Cruse CW, Blevins PK, Luce EA. Cruse CW, et al. J Trauma. 1980 Jul;20(7):551-6. doi: 10.1097/00005373-198007000-00003. J Trauma. 1980. PMID: 7392106
Slightly over one half of the group of naso-ethmoid fractures were open; the remainder were closed injuries. Traumatic telecanthus was noted in 70% of the patients on initial examination. ...
Slightly over one half of the group of naso-ethmoid fractures were open; the remainder were closed injuries. Traumatic telecanthus wa …
Diverse clinical and genetic aspects of craniofrontonasal syndrome.
Zafeiriou DI, Pavlidou EL, Vargìami E. Zafeiriou DI, et al. Pediatr Neurol. 2011 Feb;44(2):83-7. doi: 10.1016/j.pediatrneurol.2010.10.012. Pediatr Neurol. 2011. PMID: 21215906 Review.
Craniofrontonasal syndrome is characterized by coronal craniosynostosis, hypertelorism, telecanthus, a broad grooved nasal tip, dental anomalies, mild syndactyly, and broad thumbs. ...
Craniofrontonasal syndrome is characterized by coronal craniosynostosis, hypertelorism, telecanthus, a broad grooved nasal tip, denta …
Syndromic lipomatosis of the head and neck: a review of the literature.
Tadisina KK, Mlynek KS, Hwang LK, Riazi H, Papay FA, Zins JE. Tadisina KK, et al. Aesthetic Plast Surg. 2015 Jun;39(3):440-8. doi: 10.1007/s00266-015-0478-8. Epub 2015 Apr 10. Aesthetic Plast Surg. 2015. PMID: 25860506 Review.
The most common complications were hematoma and seroma in MSL, recurrence in FML, neuropraxia in CIL-F, and mild telecanthus in NLCS. CONCLUSIONS: Syndromic causes of lipomatosis are generally benign in nature but difficult to control long term. ...
The most common complications were hematoma and seroma in MSL, recurrence in FML, neuropraxia in CIL-F, and mild telecanthus in NLCS. …
Eye Abnormalities in Children with Fetal Alcohol Spectrum Disorders: A Systematic Review.
Tsang TW, Finlay-Jones A, Perry K, Grigg JR, Popova S, Cheung MMY, Bower C, Tam P, Jamieson RV, Elliott EJ. Tsang TW, et al. Ophthalmic Epidemiol. 2023 Aug;30(4):340-351. doi: 10.1080/09286586.2022.2123004. Epub 2022 Sep 14. Ophthalmic Epidemiol. 2023. PMID: 36102703 Review.
Structural and functional eye abnormalities were identified, the most prevalent being short palpebral fissure length (66.1%), visual impairment (55.5%), epicanthus (53.5%), subnormal stereoacuity (53.0%), abnormal retinal tortuosity (50.5%), impaired fixation ability (33.3%), …
Structural and functional eye abnormalities were identified, the most prevalent being short palpebral fissure length (66.1%), visual impairm …
Ocular genetic disease in the Middle East.
Khan AO. Khan AO. Curr Opin Ophthalmol. 2013 Sep;24(5):369-78. doi: 10.1097/ICU.0b013e3283638374. Curr Opin Ophthalmol. 2013. PMID: 23846189 Review.
Studies from the region have enhanced our understanding of ocular genetic conditions that are more common worldwide (such as pediatric glaucoma, pediatric cataract, and retinal dystrophy/dysfunction), rare worldwide (such as cornea plana, brittle cornea syndrome, and posterior mi …
Studies from the region have enhanced our understanding of ocular genetic conditions that are more common worldwide (such as pediatric glauc …
The Noonan syndrome.
Sanchez-Cascos A. Sanchez-Cascos A. Eur Heart J. 1983 Apr;4(4):223-9. doi: 10.1093/oxfordjournals.eurheartj.a061452. Eur Heart J. 1983. PMID: 6884370
Twenty-one patients with Noonan syndrome are presented. Telecanthus low-set ears, epicanthus and facial asymmetry were the commoner facial stigmata. ...
Twenty-one patients with Noonan syndrome are presented. Telecanthus low-set ears, epicanthus and facial asymmetry were the commoner f …
128 results