Results 61 to 70 of about 5,907 (232)

Rate of prenatal diagnosis of critical congenital heart disease continued to improve despite COVID‐19 pandemic: multicenter Canadian study

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Travel restrictions, reallocation of health resources and physical distancing during the coronavirus disease 2019 (COVID‐19) pandemic caused extraordinary strain on healthcare systems. The overall impact of public health measures during COVID‐19 on the prenatal diagnosis of congenital heart disease (CHD) has received limited ...
L. Eckersley   +13 more
wiley   +1 more source

Multiple pregnancy with complete hydatidiform mole and coexisting normal fetus: systematic review and meta‐analysis of clinical outcomes from non‐randomized studies

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Complete hydatidiform mole and coexisting normal fetus (CHMCF) is a rare condition for which there is significant heterogeneity in diagnosis, counseling and management of complications. The objective of this study was to summarize the prevalence of clinical outcomes in reported cases of CHMCF.
N. Salmeri   +8 more
wiley   +1 more source

Exercise in Pregnancy and Risk of Postpartum Depression: A Randomised Controlled Trial

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
ABSTRACT Objective To evaluate whether regular aerobic exercise during pregnancy reduces the incidence of postpartum depression in women with low‐risk singleton pregnancies. Design Single‐centre randomised controlled trial. Setting Department of Obstetrics and Gynaecology, University of Naples Federico II, Italy.
Gabriele Saccone   +6 more
wiley   +1 more source

Public Perspectives Around Prenatal Screening of Chromosomal Abnormalities: A Focus Group Study Comparing Metropolitan and Rural/Regional Areas in Australia

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, EarlyView.
ABSTRACT Background The widespread and rapid adoption of private payments for non‐invasive prenatal testing (NIPT) in Australia has introduced complexities to the decision‐making process for the public regarding prenatal screening. NIPT has the potential to be a useful screening tool, but concerns have been raised about its cost, the psychological ...
Amber Salisbury   +5 more
wiley   +1 more source

Prenatal Cell‐Free DNA Screening With Fetal Enrichment Enables Sampling From 8 Weeks of Gestational Age

open access: yesClinical Genetics, EarlyView.
Fetal fraction (FF) estimates for 170 male pregnancies sampled between 7w0d and 9w6d of GA as a function of gestational age at blood draw without (blue triangles) and with fetal enrichment (red dots). Regression lines are shown (gray 95% CI). Besides, there is a closer look at samples below 4% FF.
Seyedeh Saideh Daryabari   +6 more
wiley   +1 more source

Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion

open access: yesBalkan Journal of Medical Genetics, 2016
Chromosome 13 is one of the acrocentric chromosomes of the human karyotype. Acrocentric chromosomes are the most variable chromosomes in the human karyotype and these variations appear to have no clinical consequences.
Uzun I   +5 more
doaj   +1 more source

Valor preditivo do resultado fetal da dopplervelocimetria de ducto venoso entre a 11ª e a 14ª semanas de gestação Predictive value for fetal outcome of Doppler velocimetry of the ductus venosus between the 11th and the 14th gestation week

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2008
OBJETIVO: estudar o valor da dopplervelocimetria do ducto venoso (DV) entre a 11º e a 14º semanas de gestação, associado à medida da translucência nucal (TN), na detecção de resultado fetal adverso.
Carlos Alberto Gollo   +4 more
doaj   +1 more source

Diagnosis and management of fetal nuchal translucency

open access: yesSeminars in Roentgenology, 1998
Fetal nuchal translucency can be measured in most pregnant women in the first and early second trimester. The size of translucency varies slightly with gestational age and crown rump length and is independent of maternal age. Most authors have used a nuchal thickness of > or = 2.5 mm or > or = 3 mm to define abnormal, although some have suggested that ...
Marc Jackson, Nancy C. Rose
openaire   +3 more sources

Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher   +6 more
wiley   +1 more source

Maternal Primary Sjögren's Syndrome Complicated by Irreversible Fetal Third‐Degree Congenital Heart Block: A Case Report From Nepal

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT In pregnancies of anti‐Ro/SSA– and anti‐La/SSB–positive women with primary Sjögren's syndrome, third‐degree fetal congenital heart block is usually irreversible despite corticosteroids. Preconception counseling, hydroxychloroquine prophylaxis, and serial fetal echocardiography from 16 weeks are essential to enable timely counseling, including ...
Priety Shah   +4 more
wiley   +1 more source

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