Results 151 to 160 of about 423,772 (336)
Abstract Objective Early detection of hypoxic–ischemic encephalopathy (HIE) in neonates is critical. We conducted a pilot cohort study to determine the feasibility of collecting umbilical cord blood samples for neurofilament light (NfL) and to assess the association of NfL with non‐reassuring fetal status and other cord biomarkers. We aimed to address (
David Zalcberg +17 more
wiley +1 more source
Background: Prenatal ultrasound has always been difficult to classify fetal corpus callosum abnormalities. This paper aims to evaluate the added value of fetal magnetic resonance imaging (MRI) to ultrasound in detecting fetal corpus ...
Hui Peng +5 more
doaj +1 more source
A unique case of prenatal diagnosis of vascular Ehlers‐Danlos syndrome
Abstract We present a rare instance of prenatal diagnosis of vEDS without a family history. The suspicion of a genetic syndrome arose from an incidental ultrasound finding of a facial anomaly—previously associated with vEDS in adulthood but never described prenatally.
Emma Bertucci +5 more
wiley +1 more source
Duodenal atresia associated with umbilical vein varix: prenatal diagnosis by fetal ultrasonography
Duodenal atresia is the most frequent site of obstruction of the digestive tract and may be diagnosed in the prenatal stage. However, the varix of the umbilical vein is a rare entity.
Alegna de la Caridad Ochoa Hidalgo +2 more
doaj
Abstract Objective To compare the prevalence of pre‐eclampsia with and without severe features, and maternal and perinatal outcomes before and during the COVID‐19 pandemic. Methods Cross‐sectional study based on medical chart review of pregnant women admitted to a referral maternity hospital for childbirth between September 2019 to February 2020 ...
Juliana da‐Costa‐Santos +12 more
wiley +1 more source
Prenatal diagnosis of conjoined thoracopagus siameses
Multiple pregnancy has an increasing incidence, an implication could be the appearance of congenital defects, including twins linked by different anatomical areas. Although its incidence is low, its mortality is high, do to the connection of vital organs
Nery Ramona Hechavarría-Rodríguez +2 more
doaj
Prenatal ultrasound diagnosis of poland syndrome [PDF]
D'ARMIENTO, MARIA +2 more
core +1 more source
PRENATAL DIAGNOSIS OF ROBERT/SC SYNDROME IN A DIABETIC MOTHER WITH A HISTORY OF MEBENDAZOLE AND GLIBENCLAMIDE INTAKE [PDF]
The Robert/SC (pseudothalidomide) syndrome is a rare autosomal recessive disorder, associated with phocomelia and craniofacial abnormalities. An anomalous fetus with lower limb phocomelia and micromelia, lumbar myeloschisis, upper limb and ribs defects ...
رفاهی, سهیلا +2 more
core
Prenatal diagnosis and postnatal follow-up of congenitally corrected transposition of the great arteries and recurrent supraventricular tachycardia [PDF]
The prenatal sonographic diagnosis of congenitally corrected transposition of the great arteries (ccTGA), a rare form of congenital heart disease is very difficult.
Celik, I. +3 more
core +1 more source

