To investigate the parental perspectives of being confronted with an unforeseen fetal sex chromosomal aneuploidy (SCA), in light of the fact that this accidental finding is avoidable by rapid aneuploidy detection (RAD). +Methods: Exploratory qualitative interview study. We conducted 16 semi-structured interviews with parents who decided to continue pregnancy after the unforeseen finding of a fetal SCA. +Results: The communication of the unforeseen finding of SCA; the informed decision-making process concerning the pregnancy follow-up and the child and its future were the extracted themes. Parents were not prepared to accidental findings in routine prenatal diagnostics. All started an unguided search on the Internet. It is not at all clear w...
The study's aim was to evaluate how information related to a prenatal diagnosis of fetal malformatio...
Objective: To provide qualitative empirical data on parental expectations of diagnostic prenatal gen...
PURPOSE: The aim of this study was to compare rates of genetic counseling, invasive prenatal diagnos...
OBJECTIVE: To investigate the parental perspectives of being confronted with an unforeseen fetal sex...
OBJECTIVE: Incidental findings in prenatal diagnostic testing may or may not have clear prognostic s...
Aim: According to the published work, pregnancy termination rates due to prenatal diagnosis of fetal...
Objective: To analyse parental decisions regarding pregnancies with sex chromosome abnormalities (SC...
Problem: Fetal diagnoses are possible by the 16th week of gestation. Websites, social media, and mob...
Objectives With advancement of technology in genetic testing and widespread use of prenatal diagnos...
Objective To explore parental experiences of whole exome sequencing (WES) for prenatal diagnosis an...
Our aim was to assess patient opinions on prenatal genetic testing to determine which health risks, ...
Often the first indication that something may be wrong in a seemingly normal pregnancy occurs during...
Purpose We surveyed parents to ascertain interest in newborn genomic testing and determine whether t...
Background: Improved prenatal screening has resulted in significantly more parents facing a diagnosi...
Published online : 28 July 2020PURPOSE:To explore parental experiences of ultrarapid genomic testing...
The study's aim was to evaluate how information related to a prenatal diagnosis of fetal malformatio...
Objective: To provide qualitative empirical data on parental expectations of diagnostic prenatal gen...
PURPOSE: The aim of this study was to compare rates of genetic counseling, invasive prenatal diagnos...
OBJECTIVE: To investigate the parental perspectives of being confronted with an unforeseen fetal sex...
OBJECTIVE: Incidental findings in prenatal diagnostic testing may or may not have clear prognostic s...
Aim: According to the published work, pregnancy termination rates due to prenatal diagnosis of fetal...
Objective: To analyse parental decisions regarding pregnancies with sex chromosome abnormalities (SC...
Problem: Fetal diagnoses are possible by the 16th week of gestation. Websites, social media, and mob...
Objectives With advancement of technology in genetic testing and widespread use of prenatal diagnos...
Objective To explore parental experiences of whole exome sequencing (WES) for prenatal diagnosis an...
Our aim was to assess patient opinions on prenatal genetic testing to determine which health risks, ...
Often the first indication that something may be wrong in a seemingly normal pregnancy occurs during...
Purpose We surveyed parents to ascertain interest in newborn genomic testing and determine whether t...
Background: Improved prenatal screening has resulted in significantly more parents facing a diagnosi...
Published online : 28 July 2020PURPOSE:To explore parental experiences of ultrarapid genomic testing...
The study's aim was to evaluate how information related to a prenatal diagnosis of fetal malformatio...
Objective: To provide qualitative empirical data on parental expectations of diagnostic prenatal gen...
PURPOSE: The aim of this study was to compare rates of genetic counseling, invasive prenatal diagnos...