Mostrar registro simples

dc.contributor.authorPeña Duque, Julio Alejandropt_BR
dc.contributor.authorFerreira, Charles Franciscopt_BR
dc.contributor.authorZáchia, Suzana de Azevedopt_BR
dc.contributor.authorSanseverino, Maria Teresa Vieirapt_BR
dc.contributor.authorKessler, Rejane Guspt_BR
dc.contributor.authorMagalhães, Jose Antonio de Azevedopt_BR
dc.date.accessioned2020-12-17T04:09:41Zpt_BR
dc.date.issued2019pt_BR
dc.identifier.issn1415-4757pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/216598pt_BR
dc.description.abstractABSTRACT Trisomy 18 (T18) and trisomy 13 (T13) are polymalformative syndromes associated with a high rate of spontaneous abortions, intrauterine death, and short postnatal life. This study describes the overall outcome in a country where the therapeutic interruption of pregnancy is not available. The medical records of women with prenatal diagnosis of full trisomy of T13 or T18 between October 1994 and October 2017 were analyzed in order to describe their natural outcomes. Thirteen cases of T13 and 29 cases of T18 were included. The miscarriage rate was 9% for T18 and no cases for T13. Intrauterine fetal death occurred in 46% and 52% of cases for T13 and T18, respectively. The rate of live births for T13 was 54%, and the median survival was one day (95% CI -33.55 - 90.40) and 71% died in the first 24 hours of life. The rate of live births for T18 was 37% and the median survival was two days (95% CI -1.89 - 13.17); 90% of the affected babies died within first week of life. For the affected babies reaching the first year of life and for those who lived longer, multiple invasive and expensive procedures were required, without success in prolonging life beyond 180 days. This large series provides information for professionals and women regarding the natural histories of T13 and T18. Results of this study are consistent with those referenced in the literature, emphasizing the need of structured protocols and guidelines aiming early T13 and T18 diagnosis, prenatal care, gestation/parents follow-up, and counseling processes. For those couples with earlier diagnosis, a better follow-up and counseling during the prenatal care lead to the option for a support or palliative management of the newborn. Finally, when the counseling process is appropriate, it becomes easier to take decisions respecting the parent’s autonomy and to look for better outcomes for both, the mother and the fetus.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofGenetics and molecular biology. vol. 42, no. 1, suppl. 1 (2019), p. 286-296pt_BR
dc.rightsOpen Accessen
dc.subjectSíndrome da trissomia do cromossomo 13pt_BR
dc.subjectNatural histroy of trisomyen
dc.subjectTrisomy 13en
dc.subjectSíndrome da trissomía do cromossomo 18pt_BR
dc.subjectTrisomy 18en
dc.subjectDiagnóstico pré-natalpt_BR
dc.subjectPrenatal diagnosisen
dc.subjectAconselhamento genéticopt_BR
dc.subjectGenetic counselingen
dc.titleThe natural history of pregnancies with prenatal diagnosis of Trisomy 18 or Trisomy 13 : retrospective cases of a 23-year experience in a Brazilian public hospitalpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001119661pt_BR
dc.type.originNacionalpt_BR


Thumbnail
   

Este item está licenciado na Creative Commons License

Mostrar registro simples