PRENATAL

作品数：206被引量：309H指数：10
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相关领域：医药卫生更多>>
相关作者：赵玫施明刘立中季春鹏吴少伟更多>>
相关机构：北京大学安徽医科大学昆明市儿童医院开滦总医院更多>>
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相关基金：国家自然科学基金国家重点基础研究发展计划北京市自然科学基金中国博士后科学基金更多>>
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Prenatal multiple micronutrient-fortified balanced energy-protein supplementation and newborn telomere length and mitochondrial DNA content:a randomized controlled efficacy trial in rural Burkina Faso
《Food Science and Human Wellness》2025年第4期1387-1397,共11页Giles T.Hanley-Cook Yuri Bastos-Moreira Dries S.Martens Trenton Dailey-Chwalibóg Laeticia Celine Toe Brenda de Kok Lionel OIivier Ouédraogo Alemayehu Argaw Kokeb Tesfamariam Patrick Kolsteren Lieven Huybregts Tim S.Nawrot Sarah De Saeger Marthe De Boevre Carl Lachat 
supported by the Bill&Melinda Gates Foundation(OPP1175213);supported by the Research Foundation Flanders(12X9620N and 12X9623N);the European Research Council(ERC)under the European Union’s Horizon 2020 research and innovation program(946192,HUMYCO)。
Background:Evidence regarding the effectiveness of prenatal nutritional supplements has mainly considered anthropometric pregnancy outcomes.The effect on markers of health and disease,such as offspring telomere length...
关键词：Balanced-energy protein Burkina Faso Iron-folic acid Mitochondrial DNA Multiple micronutrients Randomized controlled trial Telomere length 
Identifying a novel SRCAP variant in floating-harbor syndrome and prenatal genetic diagnosis in this Chinese family:A case report
《World Journal of Clinical Cases》2025年第20期49-56,共8页Xiao Xiao Ping Wang He Wang Han-Bing Xie Shan-Ling Liu 
Supported by National Key Research and Development Program of China,No.2022YFC2703302.
BACKGROUND Floating-harbor syndrome(FHS)is a rare genetic disorder caused by pathogenic variants in the SRCAP gene.Most individuals with FHS have short stature,delayed speech and language development,and dysmorphic fa...
关键词：Floating-harbor syndrome SRCAP gene Exome sequencing Prenatal genetic diagnosis Sanger sequencing Case report 
Prenatal ultrasonography and genetic analysis of fetal cleidocranial dysplasia:A case report
《World Journal of Clinical Cases》2025年第10期28-34,共7页Feng Wang Pei-Feng Dai Wen-Juan Gao 
Supported by Science and Technology Development Plan Project of Weifang,No.2023YX005。
BACKGROUND Cleidocranial dysplasia(CCD)is an infrequent clinical condition with an autosomal dominant inheritance pattern.It is characterized by abnormal clavicles,patent sutures and fontanelles,supernumerary teeth,an...
关键词：Cleidocranial dysplasia Genetic analysis Ultrasonic diagnosis PRENATAL Case report 
Advancements in prenatal diagnosis and management of hypoplastic left heart syndrome:A multidisciplinary approach and future directions
《World Journal of Cardiology》2025年第3期25-40,共16页Syed Faqeer Hussain Bokhari Syed M Faizan Sattar Umair Mehboob Muhammad Umais Muhammad Ahmad Ahmad Malik Danyal Bakht Asma Iqbal Wahidullah Dost 
Hypoplastic left heart syndrome is a severe congenital defect involving underdeveloped left-sided cardiac structures,leading to significant mortality and morbidity.Prenatal diagnosis using fetal ultrasound and echocar...
关键词：Congenital disorder CARDIOLOGY Hypoplastic left heart syndrome Fetal ultrasound Congenital heart disease 
Clinical indications and Z-score-assisted NIPT testing:a new perspective in prenatal lscreening
《Gynecology and Obstetrics Clinical Medicine》2025年第1期42-50,共9页Runling Zhang Haiying Zhang Lin Zhang Xiangsha Kong Wei Wang Yuyuan Jia Meihong Ren Yan Liu Ling Zhu Hongsong Chen Huiying Rao 
Objective We aim to explore positive predictive value(PPV)in non-invasive prenatal testing(NIPT)-positive case and investigate the impact of diverse clinical indications and Z-scores on PPV performance.Methods From Ja...
关键词：prenatal screening non invasive prenatal testing prenatal diagnostic karyotyp analysis fluorescence situ hybridisation f z score nextseq cn platformpositive positive predictive value positive predictive value ppv 
Susceptible Windows of Prenatal Ozone Exposure and Preterm Birth:A Hospital-Based Observational Study
《Biomedical and Environmental Sciences》2025年第2期255-260,I0001-I0004,共10页Rongrong Qu Dongqin Zhang Hanying Li Jiayin Zhi Yanxi Chen Ling Chao Zhenzhen Liang Chenguang Zhang Weidong Wu Jie Song 
supported by the Natural Science Foundation of Henan Province[grant number:242300420115];Key Scientific Research Projects in Universities of Henan Province[grant number:23A330006].
Preterm birth(PTB)is defined as delivery before 37 weeks of gestation.PTB is associated with increased cardiovascular risk,neurodevelopmental disorders,and other diseases in infancy,childhood,and adulthood[1].Globally...
关键词：WINDOWS INDIVIDUAL annually 
Sex dimorphic associations of Prader–Willi imprinted gene expressions in umbilical cord with prenatal and postnatal growth in healthy infants
《World Journal of Pediatrics》2025年第1期100-112,共13页Berta Mas‑Parés Gemma Carreras‑Badosa Ariadna Gómez‑Vilarrubla Antonio De Arriba‑Munoz Olivia Lafalla‑Bernard Anna Prats‑Puig Francis De Zegher Lourdes Ibañez Andrea MHaqq Judit Bassols Abel Lopez‑Bermejo 
supported by grants from the Ministerio de Ciencia e Innovacion,Instituto de Salud Carlos Ⅲ(ISCⅢ),Madrid,Spain(PI19/00451 and PI22/00366 to LBA and PI20/00399 and PI23/00545 to BJ);project co-funded by FEDER(Fondo Europeo de Desarrollo Regional);funded by the grant INVESTAEP edition 2019 from the Spanish Pediatric Association.
Background The impact of Prader–Willi syndrome(PWS)domain gene expression on the growth of healthy children is not well understood.This study investigated associations between PWS domain gene expression in umbilical ...
关键词：Gene expression IMPRINTING Postnatal growth Prader-Willi syndrome Sexual dimorphism 
The gut-liver axis mechanism of increased susceptibility to non-alcoholic fatty disease in female offspring rats with prenatal caffeine exposure
《Food Science and Human Wellness》2024年第6期3522-3535,共14页Qian Wang Xiaoqian Lu Wen Hu Cong Zhang Kexin Liu Kai Tong Kaiqi Chen Hui Wang 
funded by the National Natural Science Foundation of China (82030111, U23A20407);the National Key Research and Development Program of China (2020YFA0803900);the Major Technological Innovation Projects of Hubei Province (2019ACA140);Hubei Province's Outstanding Medical Academic Leader program;the Basic and Clinical Medical Research Joint Fund of Zhongnan Hospital, Wuhan University (ZNLH202208)
Caffeine intake during pregnancy is common,while its effect on gut microbiota composition of offspring and the relationship with susceptibility to adult diseases remains unclear.This study aimed to confirm the effects...
关键词：Pregnancy CAFFEINE Gut microbiota Butyric acid Non-alcoholic fatty liver disease 
Prenatal and postnatal imaging of osteogenesis imperfecta: a case report
《镜湖医学》2024年第2期56-57,16,共3页IP Lao Hong LI Jun 
Introduction.Osteogenesis imperfecta(OI),also known as brittle bone disease,is a phenotypically diverse disorder due to deficiencies in the synthesis of type I collagen.OI is a disease characterized by brittle bones a...
关键词：imperfect SKELETAL bones 
Associating prenatal phthalate exposure with childhood autistic traits:Investigating potential adverse outcome pathways and the modifying effects of maternal vitamin D
《Eco-Environment & Health》2024年第4期425-435,共11页Hui Gao Cheng Zhang Beibei Zhu Menglong Geng Juan Tong Zixiang Zhan Yi Zhang De Wu Kun Huang Fangbiao Tao 
supported by the Joint Funds of the National Natural Science Foundation of China (No.U22A20361);the Research Project for Outstanding Young People in Universities of Anhui Province (No.2023AH030118);the National Natural Science Foundation of China (No.82103856);funds from the MOE Key Laboratory of Population Health Across Life Cycle (No.JK20204).
The association between prenatal phthalate mixture exposure and the risk of autism spectrum disorder(ASD)in children,as well as the potential mechanism and impact of maternal vitamin D,remains unclear.We analyzed data...
关键词：Autism spectrum disorder PHTHALATE Adverse outcome pathway Vitamin D Prospective birth cohort 
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