ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup +4 more
wiley +1 more source
Evaluating the Clinical Utility of Genomic Sequencing After Perinatal Death. [PDF]
Schubert CM +7 more
europepmc +1 more source
A protocol for a systematic review of standardised tools used in perinatal death review programmes. [PDF]
O'Connor E +3 more
europepmc +1 more source
Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios
ABSTRACT Objective To evaluate the diagnostic yield of exome sequencing (ES) in isolated polyhydramnios. Methods This retrospective study included 40 cases of isolated polyhydramnios. All patients underwent screening for gestational diabetes mellitus (GDM) and chromosomal microarray analysis (CMA).
Vered Offen Glassner +11 more
wiley +1 more source
Editorial: Updates on the Neuropathology of Sudden Unexplained Perinatal Death and Other Neurodevelopmental Disorders. [PDF]
Lavezzi AM, Abdala AP, Fifer WP.
europepmc +1 more source
Perinatal Death from Foetal Exsanguination [PDF]
A P, MITCHELL +2 more
openaire +2 more sources
Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections
ABSTRACT Objective We aimed to characterize the fetal features across gestation and describe genotype‐phenotype correlations for pregnancies with fetal RASopathies that were more severely affected as they presented with at least one abnormal fluid collection.
Natalie B. Gulrajani +17 more
wiley +1 more source
Management of Subsequent Pregnancy After Perinatal Death: Results from the UNSURENESS Study. [PDF]
Ravaldi C +4 more
europepmc +1 more source
Moderate Diagnostic Yield of Exome Sequencing in Fetal Growth Restriction: Retrospective Insights
ABSTRACT Objective To determine whether invasive genetic testing should be systematically proposed in cases of FGR. Methods Descriptive retrospective study of 159 FGR cases (defined by an estimated fetal growth < 3rd percentile, regardless of Doppler findings) managed at the Toulouse Fetal Medicine Center (TFMC) during 2022–2023.
Maud Langeois +5 more
wiley +1 more source
Facilitators and barriers to the implementation of maternal and perinatal death surveillance and response in Ethiopia: a systematic review. [PDF]
Yuya M +6 more
europepmc +1 more source

