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

Year Number of Results
1990 2
1991 1
1996 1
2000 1
2001 1
2010 1
2011 2
2012 1
2013 5
2014 5
2015 5
2016 13
2017 7
2018 2
2019 1
2020 6
2021 4
2022 5
2023 5

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Page 1
Interdisciplinary care of children with trisomy 13 and 18.
Weaver MS, Anderson V, Beck J, Delaney JW, Ellis C, Fletcher S, Hammel J, Haney S, Macfadyen A, Norton B, Rickard M, Robinson JA, Sewell R, Starr L, Birge ND. Weaver MS, et al. Am J Med Genet A. 2021 Mar;185(3):966-977. doi: 10.1002/ajmg.a.62051. Epub 2020 Dec 31. Am J Med Genet A. 2021. PMID: 33381915 Review.
Children with trisomy 13 and 18 (previously deemed "incompatible with life") are living longer, warranting a comprehensive overview of their unique comorbidities and complex care needs. This Review Article provides a summation of the recent literature, informed by t …
Children with trisomy 13 and 18 (previously deemed "incompatible with life") are living longer, warranting a comprehensive ove …
Holoprosencephaly.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B13-B16. doi: 10.1016/j.ajog.2020.08.178. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168217 Review. No abstract available.
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.
Rose NC, Barrie ES, Malinowski J, Jenkins GP, McClain MR, LaGrave D, Leung ML; ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.net. Rose NC, et al. Genet Med. 2022 Jul;24(7):1379-1391. doi: 10.1016/j.gim.2022.03.019. Epub 2022 May 24. Genet Med. 2022. PMID: 35608568 Free article. Review.
METHODS: Medline (PubMed) and Embase were used to identify studies examining detection of Down syndrome (T21), trisomy 18 (T18), trisomy 13 (T13), sex chromosome aneuploidies, rare autosomal trisomies, copy number variants, and maternal conditions, as …
METHODS: Medline (PubMed) and Embase were used to identify studies examining detection of Down syndrome (T21), trisomy 18 (T18 …
Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.
Taylor-Phillips S, Freeman K, Geppert J, Agbebiyi A, Uthman OA, Madan J, Clarke A, Quenby S, Clarke A. Taylor-Phillips S, et al. BMJ Open. 2016 Jan 18;6(1):e010002. doi: 10.1136/bmjopen-2015-010002. BMJ Open. 2016. PMID: 26781507 Free PMC article. Review.
ELIGIBILITY CRITERIA FOR SELECTING STUDIES: English language journal articles describing case-control studies with 15 trisomy cases or cohort studies with 50 pregnant women who had been given NIPT and a reference standard. ...CONCLUSIONS: NIPT using cell-free fetal DNA has …
ELIGIBILITY CRITERIA FOR SELECTING STUDIES: English language journal articles describing case-control studies with 15 trisomy cases o …
A tumor profile in Patau syndrome (trisomy 13).
Satgé D, Nishi M, Sirvent N, Vekemans M, Chenard MP, Barnes A. Satgé D, et al. Am J Med Genet A. 2017 Aug;173(8):2088-2096. doi: 10.1002/ajmg.a.38294. Epub 2017 May 25. Am J Med Genet A. 2017. PMID: 28544599 Review.
However, for Patau syndrome (constitutional trisomy 13), which occurs in 1/10,000-1/20,000 live births, the tumor profile has not been well characterized. ...The small number of reported malignant tumors suggests that there is not an increased risk of cancer …
However, for Patau syndrome (constitutional trisomy 13), which occurs in 1/10,000-1/20,000 live births, the tumor profi …
Cardiac Surgery in Trisomy 13 and 18: A Guide to Clinical Decision-Making.
Carvajal HG, Callahan CP, Miller JR, Rensink BL, Eghtesady P. Carvajal HG, et al. Pediatr Cardiol. 2020 Oct;41(7):1319-1333. doi: 10.1007/s00246-020-02444-6. Epub 2020 Sep 14. Pediatr Cardiol. 2020. PMID: 32924070 Review.
There has been substantial controversy regarding treatment of congenital heart defects in infants with trisomies 13 and 18. Most reports have focused on surgical outcomes versus expectant treatment, and rarely there has been an effort to consolidate existing evidence into …
There has been substantial controversy regarding treatment of congenital heart defects in infants with trisomies 13 and 18. Most repo …
Management of Children with the Trisomy 18 and Trisomy 13 Syndromes: Is there a Shift in the Paradigm of Care?
Carey JC. Carey JC. Am J Perinatol. 2021 Sep;38(11):1122-1125. doi: 10.1055/s-0041-1732363. Epub 2021 Jul 26. Am J Perinatol. 2021. PMID: 34311488 Review.
OBJECTIVE: The conventional view toward the management of infants with the trisomy 18 and trisomy 13 syndromes has been to recommend pure comfort care and the avoidance of technological interventions. ...KEY POINTS: . The conventional approach to the treatmen …
OBJECTIVE: The conventional view toward the management of infants with the trisomy 18 and trisomy 13 syndromes has been …
Trisomy 13 and 18: Selecting the road previously not taken.
McCaffrey MJ. McCaffrey MJ. Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):251-6. doi: 10.1002/ajmg.c.31512. Epub 2016 Aug 13. Am J Med Genet C Semin Med Genet. 2016. PMID: 27519759 Review.
Despite such evidence, arguments of beneficence, quality of life and limited resources are invoked to make the case to limit care to trisomy children. Lessons learned in our ignominious history with Down syndrome should guide us as we explore care for patients with …
Despite such evidence, arguments of beneficence, quality of life and limited resources are invoked to make the case to limit care to tris …
Prenatal reflex DNA screening for trisomy 21, 18 and 13.
Wald NJ. Wald NJ. Expert Rev Mol Diagn. 2018 May;18(5):399-401. doi: 10.1080/14737159.2018.1462703. Epub 2018 Apr 24. Expert Rev Mol Diagn. 2018. PMID: 29633889 Review. No abstract available.
Surveillance guidelines for children with trisomy 13.
Kepple JW, Fishler KP, Peeples ES. Kepple JW, et al. Am J Med Genet A. 2021 May;185(5):1631-1637. doi: 10.1002/ajmg.a.62133. Epub 2021 Mar 11. Am J Med Genet A. 2021. PMID: 33709620 Review.
Trisomy 13 is one of the three most common aneuploidy syndromes in live-born infants. ...The goal of this review is to present a comprehensive description of complications in children with trisomy 13 to aid in the development of monitoring and treatmen …
Trisomy 13 is one of the three most common aneuploidy syndromes in live-born infants. ...The goal of this review is to present …
57 results