Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era

In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21. In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21.

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Bibliographische Detailangaben
Veröffentlicht in:	Clinical case reports 2020-08, Vol.8 (8), p.1461-1466
Hauptverfasser:	Vervecken, Evy, Blaumeiser, Bettina, Vanderheyden, Tina, Hauspy, Jan, Janssens, Katrien
Format:	Artikel
Sprache:	eng
Schlagworte:	amniocentesis Case Report Case Reports Chromosomes deletion chromosome 13 Deoxyribonucleic acid DNA Fetuses Genomes Genotype & phenotype holoprosencephaly Intellectual disabilities invasive prenatal diagnosis Laboratories NIPT noninvasive prenatal test Placenta Pregnancy Ultrasonic imaging
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Beschreibung
Zusammenfassung:	In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21. In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21.
ISSN:	2050-0904 2050-0904
DOI:	10.1002/ccr3.2889