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Currently, prenatal diagnosis of genetic disorders requires chorionic villus sampling or amniocentesis carried out after 11 and 16 weeks of gestation, respectively. Celocentesis is a procedure for prenatal diagnosis that… Click to show full abstract
Currently, prenatal diagnosis of genetic disorders requires chorionic villus sampling or amniocentesis carried out after 11 and 16 weeks of gestation, respectively. Celocentesis is a procedure for prenatal diagnosis that could be used from as early as 7 weeks. The present investigation evaluated the feasibility of performing diagnosis for monogenic diseases using celomic fluid containing cells of fetal origin.
Keywords:
aneuploidy diagnosed;
diagnosis;
fetal aneuploidy;
celocentesis early;
prenatal diagnosis;
diagnosed celocentesis
Journal Title: Acta Obstetricia et Gynecologica Scandinavica
Year Published: 2018
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Journal Title: Acta Obstetricia et Gynecologica Scandinavica
Year Published: 2018
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!