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

Year Number of Results
1970 3
1971 2
1972 3
1973 2
1974 3
1975 4
1976 2
1977 4
1980 1
1981 2
1984 4
1985 5
1986 5
1987 5
1988 2
1989 3
1990 1
1991 3
1992 7
1993 1
1994 8
1995 6
1996 3
1997 2
1998 4
1999 4
2000 3
2001 11
2002 6
2003 4
2004 4
2005 7
2006 8
2007 8
2008 4
2009 2
2010 6
2011 2
2012 8
2013 10
2014 6
2015 7
2016 5
2017 9
2018 9
2019 14
2020 10
2021 14
2022 8
2023 8
2024 3

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247 results

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Page 1
Cat-Eye Syndrome: A Report of Two Cases and Literature Review.
Gaspar NS, Rocha G, Grangeia A, Soares HC. Gaspar NS, et al. Cureus. 2022 Jun 25;14(6):e26316. doi: 10.7759/cureus.26316. eCollection 2022 Jun. Cureus. 2022. PMID: 35911297 Free PMC article.
Cat-eye syndrome is a rare genetic disease that involves the proximal long (q) arm of chromosome 22. ...Association with congenital heart disease is also frequent and its diagnosis should raise suspicion of a genetic condition. We describe two cases of male i
Cat-eye syndrome is a rare genetic disease that involves the proximal long (q) arm of chromosome 22. ...Association wit
Cat eye syndrome caused by 22q11.1q11.21 duplication: case report in a Chinese family.
Wang Y, Zhang P, Chai Y, Zang W. Wang Y, et al. Mol Cytogenet. 2023 Oct 25;16(1):28. doi: 10.1186/s13039-023-00660-2. Mol Cytogenet. 2023. PMID: 37880750 Free PMC article.
Chromosome copy number variation analysis also showed a 1.55 Mb duplication in the 22q11.1q11.21 region of chromosome 22 in the proband's mother. Ultimately, both members of this family were diagnosed with cat eye syndrome. CONCLUSION: Cat eye
Chromosome copy number variation analysis also showed a 1.55 Mb duplication in the 22q11.1q11.21 region of chromosome 22 in the proband's mo …
Cat eye syndrome.
Sharma D, Murki S, Pratap T, Vasikarla M. Sharma D, et al. BMJ Case Rep. 2014 May 19;2014:bcr2014203923. doi: 10.1136/bcr-2014-203923. BMJ Case Rep. 2014. PMID: 24842361 Free PMC article.
Karyotyping showed an extra small marker chromosome suggestive of the Cat eye syndrome....
Karyotyping showed an extra small marker chromosome suggestive of the Cat eye syndrome....
[Cat eye syndrome].
Bremond-Gignac D, Morin G, Jedraszak G, Receveur A, Rochette J, Copin H. Bremond-Gignac D, et al. J Fr Ophtalmol. 2015 Apr;38(4):368-9. doi: 10.1016/j.jfo.2014.09.016. Epub 2015 Mar 20. J Fr Ophtalmol. 2015. PMID: 25799388 French. No abstract available.
Cat Eye Syndrome with a Unique Liver and Dermatological Presentation.
Mansur M, Jacob TJ, Wong H, Tarascin I. Mansur M, et al. Cureus. 2023 Apr 4;15(4):e37142. doi: 10.7759/cureus.37142. eCollection 2023 Apr. Cureus. 2023. PMID: 37153326 Free PMC article.
Cat eye syndrome (CES), also known as Schmid-Fraccaro syndrome, is a complex genetic syndrome with a highly variable phenotype that includes ocular coloboma, anal atresia, preauricular skin tags and pits, heart defects, kidney malformations, dysmorphic facial
Cat eye syndrome (CES), also known as Schmid-Fraccaro syndrome, is a complex genetic syndrome with a highly variable ph
[Cat-eye syndrome (a psychiatric aspect)].
Makarov IA, Gavrilina SB, Belozerov BG. Makarov IA, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(11):60-64. doi: 10.17116/jnevro201911911160. Zh Nevrol Psikhiatr Im S S Korsakova. 2019. PMID: 31851174 Russian.
Cat-eye syndrome is associated with abnormalities in chromosome 22. ...
Cat-eye syndrome is associated with abnormalities in chromosome 22. ...
Cat eye syndrome and growth hormone deficiency with pituitary anomalies: a case report and review of the literature.
Melo C, Gama-de-Sousa S, Almeida F, Rendeiro P, Tavares P, Cardoso H, Carvalho S. Melo C, et al. Gene. 2013 Oct 15;529(1):186-9. doi: 10.1016/j.gene.2013.07.031. Epub 2013 Aug 6. Gene. 2013. PMID: 23928108 Review.
Cat eye syndrome is a rare congenital disease characterized by the existence of a supernumerary chromosome derived from chromosome 22, with a variable phenotype comprising anal atresia, coloboma of the iris and preauricular tags or pits. We report a girl with
Cat eye syndrome is a rare congenital disease characterized by the existence of a supernumerary chromosome derived from
[Cat eye syndrome].
Teraoka M, Narahara K. Teraoka M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):348-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057256 Review. Japanese. No abstract available.
[Cat eye syndrome].
Kimura J. Kimura J. Ryoikibetsu Shokogun Shirizu. 2001;(33):339-40. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462464 Review. Japanese. No abstract available.
The cat-eye syndrome.
Szalay GC. Szalay GC. Am J Med Genet. 1985 Nov;22(3):633-6. doi: 10.1002/ajmg.1320220325. Am J Med Genet. 1985. PMID: 3933346 No abstract available.
247 results