Pregled bibliografske jedinice broj: 818702
Seven false-positive cases from non-invasive cell- free fetal DNA testing: Data obtained from three referring centres in Croatia
Seven false-positive cases from non-invasive cell- free fetal DNA testing: Data obtained from three referring centres in Croatia // 4th Central Eastern European Symposium on Free Nucleic Acids in Non-Invasive Prenatal Diagnosis / Paediatria Croatica, 60(Suppl.2) / Barišić, Ingeborg (ur.).
Zagreb: Klinika za dječje bolesti, 2016. str. 24-24 (predavanje, nije recenziran, sažetak, stručni)
CROSBI ID: 818702 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Seven false-positive cases from non-invasive cell-
free fetal DNA testing: Data obtained from three
referring centres in Croatia
Autori
Stipoljev, Feodora ; Crkvenac-Gornik, Kristina ; Huljev Frković, Sanda ; Gjergja-Juraški, Romana ; Brajenović-Milić, Bojana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
4th Central Eastern European Symposium on Free Nucleic Acids in Non-Invasive Prenatal Diagnosis / Paediatria Croatica, 60(Suppl.2)
/ Barišić, Ingeborg - Zagreb : Klinika za dječje bolesti, 2016, 24-24
Skup
4th Central Eastern European Symposium on Free Nucleic Acids in Non-Invasive Prenatal Diagnosis
Mjesto i datum
Split, Hrvatska, 25.05.2016. - 26.05.2016
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
aneuploidy ; cell free fetal DNA ; NIPT
Sažetak
Noninvasive prenatal testing (NIPT) using cell- free fetal DNA for screening of chromosomal aneuploidies offers high sensibility and specificity in the routine clinical praxis. However, there is stil insufficient data regarding false positive and negative cases. Both, false positive and negative results are mainlydue to the confined placental mosaicism, or vanishing twin phenomenom. A possible mosaic maternal aneuploidy can be cause of false positive result for fetal sex aneuploidy. We report seven cases with positive NIPT evaluated by chorionic villus biopsy or amniocentesis. NIPT showed high risk for two Turner syndromes, two Edwards syndromes, one triple X. one Down syndrome and one trisomy 16. All evaluated fetuses have normal karyotypes. Positive results from NIPT must always be confirmed by invasive prenatal diagnosis. In cases, were aneuploidy for X chromosome is detected, maternal cytogenetic evaluation should be considered, and offered through genetic counselling. Full information about advantages and limitation of this method is mandatory.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka,
Klinička bolnica "Sveti Duh",
Klinički bolnički centar Zagreb,
Medicinski fakultet, Osijek,
Dječja bolnica Srebrnjak
Profili:
Kristina Crkvenac
(autor)
Bojana Brajenović-Milić
(autor)
Sanda Huljev Frković
(autor)
Feodora Stipoljev
(autor)
Romana Gjergja Juraški
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus