PRENATAL DIAGNOSIS OF PALLISTER-KILLIAN SYNDROME: AN INTEGRATIVE REVIEW
DOI:
https://doi.org/10.5747/cv.2023.v15.v361Keywords:
Pallister-Killian syndrome, prenatal diagnosis, isochromosome 12p.Abstract
This article aims to report the main forms of prenatal diagnosis of Pallister-Killian Syndrome for medical purposes and to better elucidate it as well as to provide adequate genetic counseling.
It is an integrative review of a qualitative approach focused on the search for results for evidence-based practice that, after applying the inclusion criteria, the final sample consisted of 6 articles.
After analyzing and discussing them, we conclude that the present topic still needs many studies and clinical practices so that there is a pattern of screening for the Syndrome in prenatal care, however, we know that the characteristic ultrasound and genetic findings already elucidate for a better diagnostic search strategy, as well as subsequent genetic family counseling.
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