Results 1 to 10 of about 600,328 (248)

Prenatal Ultrasound Progression and Postnatal Retrospective Analysis of a Case of Small Intestinal Atresia with Volvulus [PDF]

Diagnostics
Background and Clinical Significance: Fetal jejunoileal atresia is a congenital anomaly of the lower digestive tract. Subsequent small intestinal volvulus, which may occur secondary to intestinal malrotation or atresia, represents a common cause of ...
Lilu Nong, Lei Wang, Haiqiong Luo, Yan Wang, Chunchun Chen, Jiansheng Xie, Kanglin Dai, Jun Wang, Xiaohua Xu   +8 more
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Diagnostic value of prenatal ultrasound in the typing of fetal esophageal atresia [PDF]

Frontiers in Medicine
ObjectiveTo investigate the prenatal ultrasound image features and diagnostic value of fetal esophageal atresia (EA).MethodsThe clinical and prenatal ultrasound data of 24 fetuses with suspected esophageal atresia diagnosed by prenatal ultrasound and/or ...
Lijun Song, Zhijie Zhang, Xuan Sheng, Yanjie Wang, Houmei Han, Yang Gao, Hong Yin   +6 more
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Artificial Intelligence in Prenatal Ultrasound: Clinical Application and Prospect [PDF]

Advanced Ultrasound in Diagnosis and Therapy, 2023
Since the 1990s, researchers have been seeking approaches for applying artificial intelligence (AI) to prenatal ultrasound. With the breakthrough of cloud computing technology and the development of deep learning technology, AI in prenatal ultrasound has
Wenjia Guo, MM, Shengli Li, MM, Xing Yu, MD, Huaxuan Wen, BM, Ying Yuan, MM, Xia Yang, MM
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Placental and Doppler ultrasound findings in pregnant women with SARS-CoV-2 infectionAJOG Global Reports at a Glance

AJOG Global Reports, 2023
BACKGROUND: Several viral infections cause changes in the placenta. Cytomegalovirus, herpes viruses, and HIV cause increased placental thickness; Zika virus induces focal regions of necrosis; parvovirus B19 causes a structural injury.
Eva María Soto-Sánchez, MD, PhD, Carmen López-Gorosabel, MD, PhD, Ana Belén Ibáñez-Santamaría, MD, Beatriz Sánchez-Estévez, MD, Jesús De la Fuente-Valero, MD, Juan José Hernández-Aguado, MD   +5 more
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PROGRESS IN APPLICATION OF PRENATAL ULTRASONOGRAPHY IN THE DIAGNOSIS OF SPINA BIFIDA [PDF]

精准医学杂志, 2023
Prenatal ultrasound screening plays an important role in eugenics, and the related techniques are developing rapidly. Fetal spina bifida screening is a required item for prenatal care in pregnant women. However, there is still room for improvement in its
LAI Huangyi, SUN Youxiang, JIANG Wei
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Prenatal Diagnosis of Holt–Oram Syndrome With a Novel Mutation of TBX5 Gene: A Case Report

Frontiers in Pediatrics, 2021
Background: Holt–Oram syndrome (HOS) is an autosomal dominant disorder caused by mutations of TBX5 gene.Case presentation: We report a fetus with HOS diagnosed sonographically at 23 weeks of gestation. The fetal parents are non-consanguineous.
Guan-nan He, Xue-yan Wang, Min Kang, Xi-min Chen, Na Xi, Jing Zhao, Xi Chen   +6 more
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Fetal magnetic resonance imaging in the diagnosis of spinal cord neural tube defects: A prospective study

Frontiers in Neurology, 2022
ObjectiveThis study aimed to evaluate the value of fetal magnetic resonance imaging (MRI) in the prenatal diagnosis of spinal neural tube defects.MethodsFrom August 2018 to January 2021, 56 fetuses with suspected spinal cord neural tube defects were ...
Gan Gao, Gan Gao, Benzhang Tao, Benzhang Tao, Yanyan Chen, Jiaqi Yang, Mengchun Sun, Hui Wang, Fangbin Hao, Fangbin Hao, Simeng Liu, Simeng Liu, Minjie Wang, Minjie Wang, Aijia Shang, Aijia Shang   +15 more
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Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review

Molecular Genetics & Genomic Medicine, 2023
Objective Wolf–Hirschhorn syndrome (WHS) is a congenital malformation syndrome with poor prognosis. It is associated with a heterozygous deletion of chromosome 4p16.3. Adequate knowledge of prenatal phenotypes and proper prenatal counseling are essential
Feng Tang, Yang Zeng, Li Wang, Daishu Yin, Lin Chen, Dan Xie, Jing Wang   +6 more
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Prenatal ultrasound for the diagnosis of the agenesis of corpus callosum: a meta-analysis

The Journal of Maternal-Fetal & Neonatal Medicine, 2023
Background Prenatal ultrasound has been regularly used as the screening tool for agenesis of corpus callosum (ACC) of the fetuses, which were mainly suspected on the basis of indirect signs rather than the visualization of the CC. However, the diagnostic
Yan Zhang
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Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): a case report with novel mutation

BMC Pediatrics, 2019
Background X-linked recessive chondrodysplasia punctate (CDPX1) is a rare congenital disorder of bone and cartilage development, caused by a mutation in the arylsulfatase E (ARSE) gene located on chromosome Xp22.3.
Guannan He, Yan Yin, Jing Zhao, Xueyan Wang, Jiaxiang Yang, Xi Chen, Li Ding, Yan Bai   +7 more
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