Results 71 to 80 of about 3,446 (179)
A study of maternal and fetal outcome in third trimester diagnose case of oligohydramnios [PDF]
, 2017 Background: Oligohydramnios is defined as when the maximum vertical pockets of liquor is less than 2 cm or when AFI is less than 5 cm or less than 10th centile.
Moses, Vibha, Thakre, Sarita
core +1 more source
JPGN Reports, EarlyView.Abstract We report a patient with Hoyeraal–Hreidarsson syndrome (HHS), a telomere biology disorder, who developed severe chronic enterocolitis with inflammatory bowel disease‐like features. Vedolizumab led to improvement in stool frequency, reduced fecal calprotectin, and clinical remission without infectious complications.
Yasutaka Chiba +6 more
wiley +1 more source
Prolongation of a pregnancy with second trimester severe oligohydramnios to term: a case report [PDF]
, 2019 The occurrence of oligohydramnios complicating a pregnancy is seen in 0.8 to 5.5 % of pregnancies. Severe Oligohydramnios, though not clearly defined, but clinically with an AFI of less than 5 cm appears to be an important predictor for an abnormal fetal
Paidhungat, Nitin P, Bapat, Alka C.
core +1 more source
Taiwanese Journal of Obstetrics & GynecologyObjective: The aim of this study was to investigate the value of genetic testing using exome sequencing (ES) in oligohydramnios pregnancies with or without other structural abnormalities.
Yan-Lin Li +4 more
doaj +1 more source
Genetic Investigation in Fetal Growth Restriction: An Integrated Approach for Clinical Practice
Prenatal Diagnosis, EarlyView.ABSTRACT International guidelines recommend genetic testing when fetal growth restriction (FGR) accompanies structural anomalies, but recommendations for apparently isolated FGR remain variable, particularly regarding gestational age thresholds and the role of exome sequencing (ES). Interpretation is difficult because studies define FGR inconsistently,
Eran Ashwal, David Chitayat
wiley +1 more source
Multiple abnormalities in a foetus: a possibility of multifactorial inheritance disorder
National Journal of Clinical Anatomy, 2016 A female foetus of 3.23 kg was delivered by a primigravida of 23 years, after scanning by ultrasound, depicting findings of oligohydramnios and congenital abnormalities.
D N Sinha
doaj +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To evaluate the incremental diagnostic yield of sequencing in a large, well‐phenotyped international cohort of fetuses with prenatally diagnosed agenesis of the corpus callosum (ACC) and to identify associated genes and variants. Methods Retrospective multicenter cohort study of fetuses with a prenatal diagnosis of ACC undergoing ...
Lorraine Dugoff +18 more
wiley +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To evaluate the diagnostic yield of integrated molecular autopsy (IMA) by combining deep post‐mortem phenotyping with exome (ES) and targeted genome sequencing (GS) for prenatally detected anomalies. Method This retrospective study evaluated 28 perinatal cases (22 fetuses, six neonates) with severe anomalies, normal first‐tier ...
Sihem Darouich +6 more
wiley +1 more source
, 2019 Objective: It's proposed that oligohydramnios is caused by decreased renal perfusion due to redistribution of fetal blood at fetal growth restriction.
YAPÇA, Ömer Erkan +3 more
core +1 more source
A study of perinatal outcome in patients with low Amniotic Fluid Index (AFI) [PDF]
Al Ameen Journal of Medical Sciences, 2017 Background: The amniotic fluid that surrounds the fetus is a very essential component of normal intrauterine growth. It creates a physical space for the musculoskeletal development, promotes normal lung development & helps to avert compression of the ...
Vidya A. Thobbi, Sheema Sabahath
doaj