Results 81 to 90 of about 12,731 (221)

Association of neonatal and fetal malformations with polyhydramnios and oligohydramnios - introduction of a new “association factor”

open access: yesBMC Pregnancy and Childbirth
Background Our aim was to investigate the association of different neonatal and fetal anatomical abnormalities with polyhydramnios or oligohydramnios during prenatal ultrasonography.
Artur Beke, Aténé Simonyi
doaj   +1 more source

Amniotic Fluid Volume Assessment: Eight Lessons Learned

open access: yesInternational Journal of Women's Health, 2021
Everett F Magann,1 Julie R Whittington,1 John C Morrison2 ,† Suneet P Chauhan3 1Departments of Obstetrics and Gynecology of the University of Arkansas for the Medical Sciences, Little Rock, AR, USA; 2Department of Obstetrics and Gynecology of the ...
Magann EF   +3 more
doaj  

Spectrum of Congenital Malformations in Sex Chromosome Tetrasomies and Pentasomies: A Systematic Review

open access: yesAndrology, EarlyView.
ABSTRACT Sex chromosome aneuploidies represent a heterogeneous group of chromosomal conditions, in which phenotypic complexity generally increases with the number of supernumerary sex chromosomes. While Turner syndrome and sex chromosome trisomies are relatively well characterized, less is known about congenital malformations in sex chromosome ...
Anna Colding   +3 more
wiley   +1 more source

Delivery mode and maternal health conditions before and after childbirth: A population‐based cohort study from Estonia

open access: yesActa Obstetricia et Gynecologica Scandinavica, EarlyView.
Cesarean section is associated with higher rates of chronic health conditions and pregnancy‐related complications, whereas vaginal delivery is more commonly linked to pelvic floor and perineal complications. These findings emphasize the need for individualized decision‐making and thorough counseling about the risks and benefits of each delivery method.
Katrin Täär   +13 more
wiley   +1 more source

Did Severity of Polyhydramnios affect Mode of Delivery?

open access: yesGomal Journal of Medical Sciences, 2013
Background: In Pakistan, the incidence of polyhdramnios is 2.4%. The objectives of this study were to find out the frequency of severity of polyhydramnios and the frequency of different modes of delivery in pregnancies with polyhydramnios.
Saima Perveen   +2 more
doaj  

Sickle cell anaemia with and without crises: An observational study of pregnancy outcomes

open access: yesBritish Journal of Haematology, EarlyView.
Summary We assessed the pregnancy outcomes of patients with sickle cell crises. We carried out a retrospective study of 2 698 556 pregnancies in Quebec, Canada between 1989 and 2022. The primary exposure was sickle cell anaemia with crisis during or outside of pregnancy. Outcomes included severe maternal morbidity and other pregnancy complications.
Nathalie Auger   +8 more
wiley   +1 more source

Ultrasonography for Evaluation of Polyhydramnios

open access: yes, 1997
This study was undertaken to evaluate the efficiency of ultrasonography for the prenatal assessment of Polyhydramnios. From May 1988 to October 1993, 2,320 subjects had single gestations undergoing fetal testing after 20 gestational weeks at the ...
박용원
core  

Polyhydramnios Associated with Multiple Congenital Malformations: Case Report

open access: yes, 2010
A case of polyhydramnios associated with multiple congenital abnormalities in the fetus of a 25 year old primigravida, at 33 weeks gestation is reported.
Oloyede, OAO, Lamina, MA, Adetoro, OO
core   +1 more source

Pubertal Dynamics of Sertoli and Leydig Cell Dysfunction in Klinefelter Syndrome

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Context Klinefelter syndrome (KS), defined by a 47, XXY karyotype, is commonly associated with progressive testicular failure. The precise timing of Sertoli and Leydig cell dysfunction during puberty remains unclear. Objective To determine the onset and progression of testicular insufficiency during puberty in KS, and to assess whether ...
Tredez Axelle   +9 more
wiley   +1 more source

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy

open access: yesClinical Genetics, EarlyView.
PIP5K1C‐related lethal congenital contracture syndrome with hyperinsulinism and optic atrophy. ABSTRACT Lethal congenital contracture syndrome 3 (LCCS3, MIM #611369) is a rare autosomal recessive neuromuscular disorder caused by biallelic loss‐of‐function (LOF) variants in PIP5K1C, reported in only two families to date.
Tameemi Abdalla Moady   +3 more
wiley   +1 more source

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