Results 21 to 30 of about 47,044 (172)

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

open access: yes, 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.   +3 more
core  

Placental insufficiency markers to assess the risk of non‐chromosomal genetic conditions in early‐onset fetal growth restriction

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 4, Page 492-499, April 2026.
ABSTRACT Objectives To assess the value of placental insufficiency markers for estimating the risk of genetic anomalies in fetuses with isolated early‐onset fetal growth restriction (FGR), defined as an estimated fetal weight ≤ 3rd percentile diagnosed ≤ 28 + 6 weeks' gestation.
M. Armengol‐Alsina   +17 more
wiley   +1 more source

Addition of Multi‐Level Technologies to Evaluate Eggs and Embryos and Improve Endometrial Quality Applied for In Vitro Fertilization to Achieve Pregnancy: A Case Study

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
This integrated clinical approach optimizes the reproductive cycle in several steps, starting with nutrition (A): restricting carbohydrates and inducing ketosis to reduce inflammation and improve insulin sensitivity, which benefits follicular development.
Tania G. Rojas‐Pérez   +7 more
wiley   +1 more source

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

open access: yesUltrasound 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   +8 more
wiley   +1 more source

El consejo genético prenatal [PDF]

open access: yes, 2015
Informe del Comité de Bioética de España sobre el Consejo genético prenatal emitido el 21 de enero de ...
Alonso Bedate, Carlos   +11 more
core   +1 more source

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

open access: yesJournal 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   +5 more
wiley   +1 more source

Diagnóstico prenatal de lipoma cardiaco. Presentación de un caso

open access: yesGaceta Médica Espirituana, 2015
Presentación de caso: Se presentó esta revisión con el objetivo de abordar una entidad infrecuente en el diagnóstico de las cardiopatías fetales. Se presenta un caso de un feto con una tumoración cardíaca, cuyo diagnóstico fue realizado  por estudio ...
Osvaldo Salas Requena   +2 more
doaj  

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

open access: yesInternational 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

Epignato: teratoma orofaríngeo: comunicación de un caso [PDF]

open access: yes, 2009
El epignathus es un teratoma orofaríngeo, que tiene una incidencia de 1:35000 a 1:200000 nacidos vivos. Los teratomas orofaríngeos surgen de la base del cráneo o de la pared posterior de la faringe y se extienden inferiormente causando obstrucción ...
Ambriz López, Roberto   +4 more
core  

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

open access: yesUltrasound 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   +18 more
wiley   +1 more source

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