Results 31 to 40 of about 278,563 (214)

Case Report: De novo USP9X missense mutation in a male fetus with pulmonary atresia and ventricular septal defect: expanding the genotype-phenotype spectrum of USP9X-related disorders

Frontiers in Cardiovascular Medicine
BackgroundPathogenic variants in the X-linked USP9X gene, which evades X-chromosome inactivation, have been predominantly linked to neurodevelopmental disorders (NDDs). Accumulating evidence has linked USP9X dysfunction to congenital heart disease (CHD),
Tingting Man, Tingting Man, Hairui Sun, Hairui Sun, Xiaoyan Hao, Xiaoyan Hao, Xiaowei Liu, Xiaowei Liu, Yihua He, Yihua He, Yihua He   +10 more
doaj   +1 more source

Fetal cardiac interventions: an update of therapeutic options

Brazilian Journal of Cardiovascular Surgery, 2014
Objective: This article aims to present updated therapeutic options for fetal congenital heart diseases. Methods: Data source for the present study was based on comprehensive literature retrieval on fetal cardiac interventions in terms of ...
Shi-Min Yuan
doaj   +1 more source

Prenatally diagnosed fetal heart rhythm abnormalities—incidence, diagnosis and outcome

Clinical and Experimental Obstetrics & Gynecology, 2022
Backrounds: Fetal arrhythmias represent a significant cause of fetal morbidity and mortality and occur in approximately 1–3% of pregnancies. The unknown fetal arrhythmias are the cause of intrauterine fetal demise in as many as 3–10% of cases, as well as
Jelena Stamenković, Vojislav Parezanović, Olivera Kontić-Vučinić, Ivan Stefanović, Maja Trkulja, Ida Jovanović, Aleksandar Ljubić, Milena Srbinović   +7 more
doaj   +1 more source

The Fetal Heart [PDF]

Journal of Diagnostic Medical Sonography, 1986
The purpose of this article is to inform the sonographer about how to evaluate the normal fetal heart during routine obstetric examinations. With basic knowledge of how the fetal heart should appear, a sonographer can perform an adequate basic examination in a short period of time, depending on experience. The ventricles, atria, atrioventricular valves,
openaire   +1 more source

Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34

Frontiers in Genetics, 2020
BackgroundThe NONO gene is located on chromosome Xq13.1 and encodes a nuclear protein involved in RNA synthesis, transcriptional regulation, and DNA repair.
Hairui Sun, Hairui Sun, Hairui Sun, Lu Han, Lu Han, Xiaoshan Zhang, Xiaoyan Hao, Xiaoyan Hao, Xiaoxue Zhou, Xiaoxue Zhou, Ruiqing Pan, Hongjia Zhang, Hongjia Zhang, Yihua He, Yihua He, Yihua He   +15 more
doaj   +1 more source

A review of congenital heart block [PDF]

, 2003
Congenital heart block is a rare disorder. It has an incidence of about 1 in 22,000 live births. It may be associated with high mortality and morbidity.
Glickstein, J., Buyon, Jill P., Friedman, Deborah M., Duncanson, L.J.   +3 more
core  

Maternal Cardiovascular Impairment in Pregnancies Complicated by Severe Fetal Growth Restriction

, 2012
—Fetal growth restriction and preeclampsia are both conditions of placental etiology and associated to increased risk for the long-term development of cardiovascular disease in the mother. At presentation, preeclampsia is associated with maternal global
Thilaganathan, B, Sutherland, GR, Liberati, M, Melchiorre, K   +3 more
core   +1 more source

Noninvasive FECG for estimating the fetal heart rate [PDF]

, 2013
Decelerations of fetal heart rate have been known to be associated with fetal distress. Continuous fetal heart rate monitoring was expected to result in dramatic reduction of undiagnosed fetal hypoxia, but the outputs of FHR monitors were often ...
Millet Roig, José, Sarmiento Alvarez, Luis Omar, Luis Omar Sarmiento Alvarez, González Salvador, Alberto, Jose Millet Roig, Alberto Gonzalez Salvador, Flórez Ordónez, Yudy Natalia, Yudy Natalia Florez Ordonez   +7 more
core   +1 more source

Analysis of Genotypes and Phenotypes in Chinese Patients With Tuberous Sclerosis Complex Harboring Novel Variants of TSC1 and TSC2 Genes

International Journal of Genomics
Conclusions: This study broadens the spectrum of variants of TSC1 and TSC2 genes, reaffirming the clinical diagnosis of patients through genetic testing.
Jian Chen, Hairui Sun, Ling Han, Xiaoyan Gu, Xiaoyan Hao, Yuwei Fu, Zongjie Weng, Yi Xiong, Baomin Liu, Hongjia Zhang, Yihua He, Hong Li   +11 more
doaj   +1 more source

Fetal cardiac interventions: clinical and experimental research

Advances in Interventional Cardiology, 2016
Fetal cardiac interventions for congenital heart diseases may alleviate heart dysfunction, prevent them evolving into hypoplastic left heart syndrome, achieve biventricular outcome and improve fetal survival.
Shi-Min Yuan, Gulimila Humuruola
doaj   +1 more source