Results 201 to 210 of about 88,700 (286)

The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical Considerations

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear   +7 more
wiley   +1 more source

Fetoscopic Laser Ablation of Type II Vasa Previa—Case Report and Systematic Review

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Vasa previa is a rare but potentially fatal obstetric condition in which fetal vessels traverse the internal cervical os without the protection of placental tissue or Wharton's jelly, making them highly vulnerable to rupture during labor or spontaneous membrane rupture. This can result in rapid fetal exsanguination and death.
Rodrigo Ruano   +5 more
wiley   +1 more source

Characteristics and outcomes associated with multiple triage visits among patients with suspected preterm labor or preterm premature rupture of membranes. [PDF]

open access: yesAJOG Glob Rep
Hamilton JL   +20 more
europepmc   +1 more source

Predictors of Adverse Perinatal Outcome in Twin Anemia Polycythemia Sequence: Evidence From a Single Center Cohort Study

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the perinatal outcome of monochorionic pregnancies complicated by Twin Anemia‐Polycythemia Sequence (TAPS) and identify prognostic factors associated with adverse outcomes. Methods A retrospective study (2012–2024) analyzed TAPS cases at a tertiary center.
Keren Zloto   +5 more
wiley   +1 more source

Prenatal Diagnosis of Joubert Syndrome 23 With Left Isomerism: A Novel Phenotype Associated With Pathogenic KIAA0586 Variant

open access: yesPrenatal Diagnosis, EarlyView.
Abstract Joubert syndrome is a rare autosomal recessive ciliopathy defined by the “molar tooth” sign caused by cerebellar vermis hypoplasia and abnormal superior cerebellar peduncles. Over 40 genes are known to cause the disorder, including KIAA0586, which encodes the centrosomal protein TALPID3, essential for ciliogenesis and Hedgehog signaling ...
Tamara Casteleyn   +6 more
wiley   +1 more source

The intersection of cervicovaginal microbiota and cervical length in predicting adverse perinatal outcomes at preterm birth risk. [PDF]

open access: yesBMC Pregnancy Childbirth
Okutucu G   +7 more
europepmc   +1 more source

Placenta Position: A Sonographic Guide for Ultrasound Health Practitioners in Low‐Resource Settings Utilising a Traffic Light System

open access: yesSonography, EarlyView.
To access CPD test for this article click here: https://www.sonographers.org/cpds/Placenta_position. ABSTRACT Introduction Maternal haemorrhage from placenta praevia (PP) is a major cause of maternal and neonatal morbidity and mortality in low‐resource settings (LRS).
Ann E. Quinton   +3 more
wiley   +1 more source

Home - About - Disclaimer - Privacy