Results 41 to 50 of about 594,197 (205)

Multiple pregnancy with complete hydatidiform mole and coexisting normal fetus: systematic review and meta‐analysis of clinical outcomes from non‐randomized studies

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 3, Page 272-282, March 2026.
ABSTRACT Objective Complete hydatidiform mole and coexisting normal fetus (CHMCF) is a rare condition for which there is significant heterogeneity in diagnosis, counseling and management of complications. The objective of this study was to summarize the prevalence of clinical outcomes in reported cases of CHMCF.
N. Salmeri, A. Pizzetti, E. Grassi, R. Cioffi, G. Mangili, M. Seckl, A. Sotiriadis, M. Candiani, P. I. Cavoretto   +8 more
wiley   +1 more source

Importancia del diagnóstico prenatal de las cardiopatías congénitas

, 2018
Resumen En Mexico, la ultima estadistica del INEGI del ano 2015 muestra que la segunda causa de mortalidad infantil se debe a malformaciones congenitas las cuales en su mayoria son cardiopatias congenitas.
D. Mendoza, A. J. García, S. A. Gallegos   +2 more
semanticscholar   +1 more source

Síndrome de Pfeiffer tipo 2: diagnóstico prenatal. Reporte de caso y revisión de la literatura

Revista Peruana de Ginecología y Obstetricia, 2019
El síndrome de Pfeiffer es una enfermedad rara de tipo autosómica dominante caracterizada por craneosinostosis bicoronal, hipoplasia medio facial y sindactilia de manos y pies. Se ha descrito 3 fenotipos, siendo el tipo 2 el más severo y que generalmente
Erasmo Huertas Tacchino, Jorge La Serna-Infantes, Rosa Alvarado Merino, Jaime Ingar Pinedo, Walter Castillo Urquiaga, Mario Zárate Girao, Walter Ventura Laveriano   +6 more
semanticscholar   +1 more source

Prenatal diagnosis and follow-up of congenital splenic cysts [PDF]

, 2006
Los quistes esplénicos congénitos son entidades poco frecuentes, particularmente en la edad pediátrica. En la literatura especializada existen pocos casos publicados con diagnóstico durante el período prenatal. Los autores describen 2 casos clínicos,
Castro, J., Miguez, R., Prior, C., Teixeira, F.   +3 more
core  

Hammersmith Infant Neurological Examination at 3 Months in Infants at Risk for Congenital Infections: A Cohort Study

Journal of Paediatrics and Child Health, Volume 62, Issue 3, Page 374-380, March 2026.
ABSTRACT Introduction STORCH refers to a group of congenital infections (syphilis, toxoplasmosis, rubella, cytomegalovirus and herpes) that can impact the central nervous system. As clinical signs may not appear until several months or years after birth, the early detection of risk in STORCH‐exposed infants has been challenging, and the use of ...
Karen Cristine Oliveira de Azambuja, Amanda de Arguelho Oliveira Arguelho, Meyene Duque Weber, Lorrainy Marques da Silva Dutra, Tathiana Ghisi de Souza, Daniele Soares‐Marangoni   +5 more
wiley   +1 more source

Using artificial intelligence as a technological tool in gynecologic and obstetric health: A narrative literature review

International Journal of Gynecology &Obstetrics, Volume 172, Issue 2, Page 850-865, February 2026.
Abstract Maternal mortality remains a critical global public health issue, particularly in low‐ and middle‐income settings where failures in surveillance, early diagnosis, and clinical decision making compromise obstetric care. In this context, the present study aimed to critically review the scientific literature on the use of artificial intelligence (
Gustavo Gonçalves dos Santos
wiley   +1 more source

Evolución de los pacientes con diagnóstico cardiológico prenatal [PDF]

, 2016
Las cardiopatías congénitas tienen una incidencia de 9/1000 nacidos vivos, siendo graves en la cuarta parte de los casos. El objetivo del estudio consiste en describir las características de las pacientes remitidas a la consulta de Cardiología Perinatal ...
Gutiérrez Pérez de Lis, Ana, Sánchez Torrente, Miguel   +1 more
core  

Undetected cases after implementation of first‐trimester anomaly scan in low‐risk population: insights from the IMITAS study

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 27-33, January 2026.
ABSTRACT Objective To assess the effectiveness of the first‐trimester anomaly scan (FTAS) performed as part of a centrally steered national screening program in The Netherlands by investigating false‐negative cases with a fetal structural anomaly that was not detected at the FTAS.
K. Bronsgeest, E. E. R. Lust, S. C. E. Zaaijer, L. Henneman, N. Crombag, C. M. Bilardo, R.‐J. H. Galjaard, E. Sikkel, A. K. K. Teunissen, M. N. Bekker, M. C. Haak, Collaborators, A. B. C. Coumans, A. Elvan‐Taşpınar, S. Galjaard, A. T. J. I. Go, E. van Leeuwen, G. T. R. Manten, E. Pajkrt   +18 more
wiley   +1 more source

Valor predictivo positivo del diagnóstico prenatal invasivo para alteraciones cromosómicas

, 2018
Introduction: Invasive prenatal diagnosis (PD) for chromosomal abnormalities (CA) is performed following non-invasive tests indications and is based on the probability of finding an altered karyotype.
Andrés Fandiño-Losada, Beatriz E Lucumí-Villegas, Julián Ramírez-Cheyne, Carolina Isaza de Lourido, Wilmar Saldarriaga-Gil   +4 more
semanticscholar   +1 more source

Consequences of prenatal exposure to alcohol: Historical development of the research and evolution of the recommendations [PDF]

, 2014
Objetivo: diversos estudios señalan un déficit y una demanda de información entre distintos profesionales de la salud en relación con las características de los trastornos vinculados a la exposición prenatal al alcohol y su prevención.
Arán Filippetti, Vanessa, López, Mariana Beatríz   +1 more
core   +2 more sources