Можливості ультразвукової діагностики хромосомної патології [PDF]
У статті для оцінки хромосомної патології використовують ультразвукові маркери – комірний простір. Кращий термін вагітності для вимірювання комірцевого простору плодів є від 11 тижнів до 13 тижнів 6 днів.
Антонюк, Ольга Петрівна +2 more
core
False negative NIPT results: Risk figures for chromosomes 13,18 and 21 based on chorionic villi results in 5967 cases and literature review [PDF]
Non-invasive prenatal testing (NIPT) demonstrated a small chance for a false negative result. Since the "fetal" DNA in maternal blood originates from the cytotrophoblast of chorionic villi (CV), some false negative results will have a biological origin ...
Berg, C.D.F. (Cardi) van den +10 more
core +1 more source
In addition to its role in the assessment of risk for trisomy 21, increased nuchal translucency (NT) thickness can also identify a high proportion of other chromosomal defects and is associated with major abnormalities of the heart and great arteries, and a wide range of genetic syndromes.
Kypros H, Nicolaides, Piotr, Wegrzyn
openaire +1 more source
Relationship Between Fetal Nuchal Thickening and Crown-Rump Length in Thai Fetuses
Objective: To investigate the relationship between the Nuchal thickening (NT) and crown–rump length (CRL) in normal Thai fetuses during 10-14 weeks of gestation. Methods: A prospective observational study was conducted. Ultrasound measurement of NT and
Saifon Chawanpaiboon +3 more
doaj
Increased nuchal translucency and distended jugular lymphatic sacs on first‐trimester ultrasound [PDF]
M. N. Bekker +4 more
openalex +1 more source
Chromosomal abnormalities and fetal nuchal translucency in first trimester. [PDF]
Rüdiger Pittrof, Shamim S. Majid
openalex +1 more source
OP01.12: Karyotype and outcome of fetuses with increased nuchal translucency above 99th percentile [PDF]
Jin Hoon Chung +5 more
openalex +1 more source
Aneuploidy screening: Newer noninvasive test gains traction [PDF]
Favorable results from the 2 studies reviewed here have prompted ACOG to recommend that cell-free DNA screening be discussed with all pregnant patients. Practice changer: Discuss cell-free DNA testing when offering fetal aneuploidy screening to pregnant ...
Farahi, Narges +3 more
core
First‐trimester screening for chromosomal abnormalities by integrated application of nuchal translucency, nasal bone, tricuspid regurgitation and ductus venosus flow combined with maternal serum free β‐hCG and PAPP‐A: a 5‐year prospective study [PDF]
Saeed Reza Ghaffari +22 more
openalex +1 more source
Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening? [PDF]
Francesca Bardi +9 more
openalex +1 more source

