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What to expect after birth in idiopathic polyhydramnios? An analysis of postnatal diagnoses and their relationship to the polyhydramnios degree
PurposeTo analyze postnatal abnormalities in idiopathic polyhydramnios and to estimate whether there was an association between the severity of...
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Polyhydramnios associated with rare genetic syndromes: two case reports
BackgroundWe present two genetic causes of polyhydramnios that were challenging to diagnose due to their rarity and complexity. In view of the severe...
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Discrimination of blood metabolomics profiles in neonates with idiopathic polyhydramnios
This study aimed to compare the blood metabolic status of neonates with idiopathic polyhydramnios (IPH) and those with normal amniotic fluid, and to...
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Comparing pregnancy, childbirth, and neonatal outcomes in women with idiopathic polyhydramnios: a prospective cohort study
BackgroundIn this prospective cohort study, the perinatal outcome in idiopathic polyhydramnios compared with normal pregnancies was examined.
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Fetal pharyngeal glial heterotopia manifested as polyhydramnios: a rare case with difficult prenatal diagnosis
BackgroundGlial heterotopia is a rare congenital developmental malformation that presents as tumor-like lesions of the nerve tissue that grow outside...
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Bronchopulmonary dysplasia is associated with polyhydramnios in a scan for novel perinatal risk factors
BackgroundThe pathogenesis of bronchopulmonary dysplasia (BPD) is multifactorial, and there are limited data about prenatal exposures and risk of BPD.
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Amniotic Aaquaporins (AQP) in Normal and Pathological Pregnancies: Interest in Polyhydramnios
Polyhydramnios is a common feature diagnosed by ultrasound in the second half of pregnancy. Biochemical analysis of amniotic fluid can be useful when...
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The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnancies
PurposeTo analyze the risk for clinically significant microarray aberrations in pregnancies with polyhydramnios.
MethodsData from all chromosomal...
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A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy
BackgroundAlterations in the MYH7 gene can cause cardiac and skeletal myopathies. MYH7 -related skeletal myopathies are extremely rare, and the vast...
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Is It Diabetes or Just Macrosomia? Fetal Myocardial Performance Index in Large-for-Gestational Age Fetuses
Our aim in this study was to investigate whether there is an association between large-for-gestational age (LGA) fetuses and myocardial performance...
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Unexpected tracheal agenesis with prenatal diagnosis of aortic coarctation, lung hyperecogenicity and polyhydramnios: a case report
BackgroundTracheal agenesis (TA) is a rare disorder usually diagnosed prenatally when a congenital high airway obstruction syndrome (CHAOS) is...
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Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation
IntroductionCongenital chloride diarrhoea (CCD) is an autosomal recessive condition that causes secretory diarrhoea and potentially deadly...
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Urinary tract infection by a rare pathogen Cedecea neteri in a pregnant female with Polyhydramnios: rare case report from UAE
BackgroundCedecea neteri is a gram-negative, oxidase-negative bacillus, a rare pathogen. Few reports are emerging globally about its antimicrobial...
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Gestational Diabetes and Analysis of Maternal and Fetal Outcomes Among Pregnant Women: A Cross-Sectional Study
Purpose of the StudyTo determine the occurrence of gestational diabetes mellitus and analyze the maternal and fetal outcomes among pregnant women.
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Report and follow-up on two new patients with congenital mesoblastic nephroma
BackgroundTumors are rare in neonatal age. Congenital mesoblastic nephroma (CMN) is a usually benign renal tumor observed at birth, or in the first...
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The association between pregnancies complicated with isolated polyhydramnios or oligohydramnios and offspring long-term gastrointestinal morbidity
ObjectiveInfants born to mothers with pregnancies complicated by polyhydramnios or oligohydramnios are at an increased risk for significant adverse...
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Relationship between increased maternal serum free human chorionic gonadotropin levels in the second trimester and adverse pregnancy outcomes: a retrospective cohort study
BackgroundA retrospective cohort study was conducted to collect the data of pregnant women who received hospital delivery in Hangzhou Women's...
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Kagami–Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report
BackgroundKagami–Ogata syndrome is also known as paternal uniparental disomy 14 and related disorders and is caused by abnormal genomic imprinting in...
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Mature Cystic Oral Teratoma in a Neonate- A Case Report
Background: Neonatal oral cavity masses present complex diagnostic and management challenges, often involving respiratory distress. We present a case...
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Prenatal ultrasonic diagnosis of esophageal atresia and tracheoesophageal fistula combined with interrupted inferior vena cava: a rare case report
PurposeThis is an extremely rare case of complicated fetal esophageal atresia (EA) with tracheoesophageal fistula (TEF) and interrupted inferior vena...
