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Results by year

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

Year Number of Results
1968 2
1970 2
1971 2
1972 1
1973 3
1974 1
1975 6
1976 7
1977 7
1978 8
1979 11
1980 3
1981 12
1983 1
1984 1
1985 3
1986 11
1987 5
1988 4
1989 5
1990 11
1991 9
1992 4
1993 7
1994 6
1995 8
1996 9
1997 3
1998 8
1999 4
2000 8
2001 9
2002 2
2003 8
2004 10
2005 6
2006 10
2007 7
2008 5
2009 5
2010 9
2011 4
2012 6
2013 11
2014 7
2015 5
2016 5
2017 5
2018 11
2019 8
2020 9
2021 5
2022 4
2023 10
2024 3

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317 results

Results by year

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Page 1
Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2019 Sep;58(5):692-697. doi: 10.1016/j.tjog.2019.07.020. Taiwan J Obstet Gynecol. 2019. PMID: 31542095 Free article. Review.
OBJECTIVE: We present prenatal diagnosis of mosaic trisomy 22 at amniocentesis in a pregnancy with facial cleft, oligohydramnios and intrauterine growth restriction (IUGR), and we review the literature. ...Repeat amniocentesis at 22 weeks of gestation using uncultur …
OBJECTIVE: We present prenatal diagnosis of mosaic trisomy 22 at amniocentesis in a pregnancy with facial cleft, oligohydramni …
Trisomy 22.
Zellweger H, Ionasescu V, Simpson J. Zellweger H, et al. J Genet Hum. 1975 Mar;23(1):65-75. J Genet Hum. 1975. PMID: 1165480
Trisomy 22 is much rarer than trisomy 21. This report presents presumptive evidence that the cat eye syndrome (CES), the so-called "trisomy 22" (T22), the intermediate cases (IM) with cardinal symptoms of CES and T22, and some cases of mental retardati
Trisomy 22 is much rarer than trisomy 21. This report presents presumptive evidence that the cat eye syndrome (CES), the so-ca
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature.
Trevisan V, Meroni A, Leoni C, Sirchia F, Politano D, Fiandrino G, Giorgio V, Rigante D, Limongelli D, Perri L, Sforza E, Leonardi F, Viscogliosi G, Contaldo I, Orteschi D, Proietti L, Zampino G, Onesimo R. Trevisan V, et al. Genes (Basel). 2024 Mar 8;15(3):346. doi: 10.3390/genes15030346. Genes (Basel). 2024. PMID: 38540405 Free PMC article. Review.
BACKGROUND: Among aneuploidies compatible with life, trisomy 22 mosaicism is extremely rare, and only about 25 postnatal and 18 prenatal cases have been described in the literature so far. ...
BACKGROUND: Among aneuploidies compatible with life, trisomy 22 mosaicism is extremely rare, and only about 25 postnatal and 1 …
Liveborn trisomy 22: report of one case.
Lean SF, Lin SP, Shen EY, Ho MY, Yang SY. Lean SF, et al. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1992 May-Jun;33(3):226-30. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1992. PMID: 1514417 Review.
A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described. Physical manifestations included failure to thrive, hypotonia, pre-auricular sinus, low set ears, hypertelorism, posterior low hair line, micrognathia, cleft palate, congenita …
A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described. Physical manifestations included fa …
Trisomy 22 mechanisms.
Punnett HH, Kistenmacher ML. Punnett HH, et al. Hum Genet. 1981;56(3):421. doi: 10.1007/BF00274706. Hum Genet. 1981. PMID: 7239526 No abstract available.
Trisomy 22 mosaicism and normal developmental outcome: report of two patients and review of the literature.
Abdelgadir D, Nowaczyk MJ, Li C. Abdelgadir D, et al. Am J Med Genet A. 2013 May;161A(5):1126-31. doi: 10.1002/ajmg.a.35812. Epub 2013 Mar 25. Am J Med Genet A. 2013. PMID: 23529842 Review.
While the majority of patients with mosaic trisomy 22 had abnormal cognitive development, normal development has also been documented. It is conceivable that children with trisomy 22 mosaicism, with minimal physical findings and normal development are …
While the majority of patients with mosaic trisomy 22 had abnormal cognitive development, normal development has also been doc …
Tertiary trisomy (22q11q),47,+der(22),t(11;22).
Biederman BM, Lin CC, Lowry RB, Somerville R. Biederman BM, et al. Hum Genet. 1980 Feb;53(2):173-7. doi: 10.1007/BF00273491. Hum Genet. 1980. PMID: 7358384
The clinical findings in previously reported cases are reviewed and compared with the features of reported patients with "partial trisomy 11q" and "trisomy 22" syndromes. Half of the ten reported families had additional balanced translocation carriers who may have a …
The clinical findings in previously reported cases are reviewed and compared with the features of reported patients with "partial trisomy 11 …
Trisomy 22 mosaicism.
Mollica F, Sorge G, Pavone L. Mollica F, et al. J Med Genet. 1977 Jun;14(3):224-5. doi: 10.1136/jmg.14.3.224. J Med Genet. 1977. PMID: 881717 Free PMC article.
A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitution. ...
A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitution. .. …
Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL. Kobrynski L, et al. Am J Med Genet. 1993 Apr 1;46(1):68-71. doi: 10.1002/ajmg.1320460111. Am J Med Genet. 1993. PMID: 8494034 Review.
We report on an infant girl born with complete trisomy 22 and left hemifacial microsomia, ear anomaly, and limbal and epibulbar complex choristoma. Trisomy 22 was confirmed by prometaphase chromosome analysis and in situ hybridization. ...
We report on an infant girl born with complete trisomy 22 and left hemifacial microsomia, ear anomaly, and limbal and epibulba …
Trisomy 22.
Zellweger H, Ionasescu V, Simpson J. Zellweger H, et al. J Genet Hum. 1975 Oct;23 SUPPL:134. J Genet Hum. 1975. PMID: 1214145 No abstract available.
317 results