Results 121 to 130 of about 30,665 (241)

Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions

open access: yesPrenatal Diagnosis, Volume 46, Issue 1, Page 3-11, January 2026.
ABSTRACT Objective We describe a series of pregnancies with autosomal dominant lymphedema and generalized lymphatic dysplasia in the fetus diagnosed with prenatal exome or genome sequencing. We focus on specific syndromes, fetal features, and parental symptoms to deepen our understanding of congenital lymphatic anomalies.
Sara G. Vargo   +4 more
wiley   +1 more source

The Incremental Yield of CMA Over Karyotype in Fetal Growth Restriction—A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, Volume 46, Issue 1, Page 56-74, January 2026.
ABSTRACT The main objective of our study was to conduct a systematic literature review and a meta‐analysis to evaluate the incremental yield of chromosomal microarray analysis compared with karyotyping in cases of fetal growth restriction. Our review was designed according to the PRISMA guidelines.
Ioakeim Sapantzoglou   +8 more
wiley   +1 more source

Fetal Macrocephaly: Prenatal Findings and Follow‐Up in Cases With High Risk for Abnormal Outcome

open access: yesPrenatal Diagnosis, Volume 46, Issue 1, Page 125-137, January 2026.
ABSTRACT Objective Fetal macrocephaly (HC Z‐score ≥ +2) is a common reason for referral for neurosonography. While most cases are benign and asymptomatic, syndromic macrocephaly poses a significant risk of abnormal neurodevelopment. This study aimed to describe the sonographic and genetic features of fetuses at the highest risk of syndromic ...
Hadas Miremberg   +10 more
wiley   +1 more source

Impact of preoperative second‐trimester vaginal bleeding on operative factors and outcomes in patients undergoing laser for twin–twin transfusion syndrome

open access: yesPregnancy, Volume 2, Issue 1, January 2026.
Abstract Introduction Second‐trimester vaginal bleeding has been associated with increased risk for preterm delivery after laser for twin–twin transfusion syndrome (TTTS), but its incidence and impact on operative factors and other outcomes is unknown. Methods A retrospective analysis of prospectively collected data from a monochorionic (MC) pregnancy ...
Juliana S. Gebb   +7 more
wiley   +1 more source

Placental Echolucencies: Does Their Presence Influence Outcome following Genetic Amniocentesis? [PDF]

open access: bronze, 1996
Suzanne M. Carter   +4 more
openalex   +1 more source

Maternal decision‐making for patients offered prenatal myelomeningocele repair

open access: yesPregnancy, Volume 2, Issue 1, January 2026.
Abstract Introduction To explore the decision‐making process for patients offered prenatal myelomeningocele repair. Methods This single‐center prospective cohort study enrolled women who were candidates for prenatal myelomeningocele repair. Participants completed prenatal and postpartum interviews, which explored their understanding of the risks ...
Laura C. Colicchia   +6 more
wiley   +1 more source

Estudio genético en embarazadas> Genetic studies in pregnancies

open access: yesRevista Colombiana de Obstetricia y Ginecología, 2004
Introducción: con base en el impacto que genera el hallazgo de un feto o recién nacido con alguna alteración cromosómica, desde el punto de vista familiar, social y para las entidades de salud, se analizan los resultados de los estudios genéticos ...
Julio César Posso Álvarez   +3 more
doaj  

Reducing the Need for Amniocentesis in Women 35 Years of Age or Older with Serum Markers for Screening [PDF]

open access: bronze, 1994
James E. Haddow   +5 more
openalex   +1 more source

Anterior placenta - Does location matter in amniocentesis?

open access: diamond, 2022
Meenakshi Gothwal   +2 more
openalex   +1 more source

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