Results 81 to 90 of about 10,016 (193)
Natural History of Fetal Non‐Nuchal Lymphatic Malformations: A Single Center Retrospective Study
ABSTRACT Objective To document the natural history and complications of second‐ and third‐trimester non‐nuchal lymphatic malformations (LM) and identify predictors of these complications. Methods We conducted a single‐centre retrospective review of fetuses diagnosed with LMs between January 2015 and January 2024.
Yada Kunpalin +8 more
wiley +1 more source
ABSTRACT Objectives To evaluate alterations in fetal cardiac function in pregnancies complicated by fetal growth restriction (FGR) by synthesizing evidence on myocardial performance index (MPI) and its constituent parameters for both the left and right ventricles.
A. Sirico +4 more
wiley +1 more source
Floyd Type II Congenital Tracheal Agenesis in a Preterm Neonate: A Rare Case Report [PDF]
Tracheal agenesis is a rare and life-threatening airway malformation, and currently, there is no curative treatment available. The described case involves a preterm male newborn at 30 weeks of gestational age who could not be intubated during ...
Shikha Khandelwal +4 more
doaj +1 more source
ABSTRACT Aim We evaluated the impact of ‘CoolCuddle’, parental cuddling during therapeutic hypothermia intervention for hypoxic‐ischaemic encephalopathy, on heart rate variability (HRV). Methods In this prospective, single‐group, interventional study with repeated measures, we included infants ≥ 36 weeks' gestation undergoing hypothermia and CoolCuddle
Ela Chakkarapani +3 more
wiley +1 more source
The Burden: Hearing loss (HL) is the most prevalent sensory disorder globally, affecting 1.5 million individuals in Brazil. The Gap: While > 150 genes are linked to HL, the genetic architecture in underrepresented populations like Brazil is poorly defined. The Problem: This lack of data limits diagnostic yield and the application of precision medicine.
Stella Diogo‐Cavassana +7 more
wiley +1 more source
Prenatal Diagnosis of Bartter Syndrome: Lessons From a Complex Diagnostic Procedure
Bartter syndrome is an idiopathic condition that may manifest antenatally, characterized by a spectrum of symptoms including maternal polyhydramnios, prematurity, polyuria, hypercalciuria, nephrocalcinosis, normomagnesemia, vomiting, growth retardation ...
Athina A. Samara +9 more
doaj +1 more source
Paying attention to extremely high frequency and a huge variety of serious complications and consequences, pregnancy polyhydramnios is an important and urgent problem in obstetrics.
N. A. Gaistruk +3 more
doaj
Severe Recurrent Polyhydramnios as a Prenatal Signal of MAGED2-Related Bartter Syndrome: A Clinical Perspective. [PDF]
Engel O +6 more
europepmc +1 more source
Primary Hyperparathyroidism in a Pregnant Immigrant Facing Healthcare Hurdles: A Case Report. [PDF]
McCrary R +4 more
europepmc +1 more source

