Results 31 to 40 of about 9,229 (165)
Analysis of chromosomal karyotypes in cases of cytogenetic counseling and leukemia disea [PDF]
, 2010 目的：应用染色体分析技术对厦门地区的遗传咨询者以及白血病患者进行染色体核 型分析，以了解厦门地区染色体病发生状况、对优生优育工作提供实验依据以及通过染 色体核型分析对白血病患者的诊断、治疗和预后提供实验依据。方法：对遗传咨询者采 用外周血淋巴细胞培养法，对白血病患者采用骨髓细胞短期培养法，G显带。结果：2005 年至2008年厦门地区遗传咨询者染色体病发生率为19.11%。其中，不良孕产组的染色 体异常率为7.77%；性发育不良组的染色体异常率为25.28%；智力低下组的染色体异常 率为47.76 ...
张旺东
core
Routine 36‐week scan: diagnosis and outcome of abnormal fetal presentation
Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 2, Page 154-162, February 2025.ABSTRACT Objectives First, to report the incidence of non‐cephalic presentation at a routine 36‐week ultrasound scan, the uptake and success of external cephalic version (ECV) and the incidence of spontaneous rotation from non‐cephalic to cephalic presentation.
M. Fitiri +5 more
wiley +1 more source
磁性纳米复合粒子富集胎儿细胞在无创性产前诊断22q11.2微缺失综合征中的应用
Zhongguo shiyan zhenduanxue, 2011 目的探讨利用磁性纳米复合粒子富集胎儿细胞进行无创性产前诊断22q11.2微缺失综合征的可行性。方法收集研究对象26例,分别经过磁性纳米粒子富集胎儿有核红细胞（研究组）及羊水穿刺胎儿细胞（对照组）进行荧光原位杂交（FISH）检测确定22q11.2是否存在异常,比较两组之间存在的差异。结果两组在诊断22q11.2微缺失综合征方面一致率为100%（2/2）,证实了利用该方法实现无创性产前诊断22q11.2微缺失综合征的可行性。结论磁性纳米复合粒子富集胎儿细胞诊断22q11.2微缺失综合征为无创性的产前诊断 ...
杜迎亭 +4 more
doaj
Prevention of hemoglobinopathies in Turkey
Thalassemia Reports, 2013 Hemoglobinopathies are the most common genetic disorders in Turkey. The incidence of beta thalassemia and sickle cell trait (HbAS) is 2.0% and 0.3% respectively. In addition to HbS, 51 abnormal hemoglobins and 42 different beta thalassemia mutations have
Mehmet Akif Çürük +2 more
doaj +1 more source
Routine 36‐week scan: prediction of small‐for‐gestational‐age neonate
Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 1, Page 20-29, January 2025.ABSTRACT Objectives First, to compare the predictive performance of routine ultrasonographic estimated fetal weight (EFW) at 31 + 0 to 33 + 6 and 35 + 0 to 36 + 6 weeks' gestation for delivery of a small‐for‐gestational‐age (SGA) neonate. Second, to compare the predictive performance of EFW at 36 weeks' gestation for SGA vs fetal growth restriction ...
S. Adjahou +5 more
wiley +1 more source
Zhongguo shiyan zhenduanxue, 2012 目的探讨妊娠期糖尿病应用国际糖尿病与妊娠研究组（IADPSG）诊断标准的合理性。方法对50g糖筛查阳性孕妇进行葡萄糖耐量实验,分别根据第7版妇产科教科书及IADPSG诊断标准诊断妊娠期糖尿病并分组,取同期非妊娠期糖尿病孕妇作为对照组,比较各组间妊娠结局。结果教科书诊断标准诊断阳性率9.7%,IADPSG诊断标准诊断阳性率12.3%。,按IADPSG诊断标准属于漏诊组的剖宫产率、子痫前期、羊水过多发生率均高于对照组,新生儿窒息、新生儿低血糖、巨大儿、大于胎龄儿发生率均高于对照组 ...
芦雅苹 +4 more
doaj
Thalassemia Reports, 2014 Hemoglobinopathies (HBP) are the most common genetic disorder in Oman and are in need of prevention programs due to the high incidence of β-thalassemia major and sickle cell disease. Prenatal diagnosis (PD) and selective pregnancy termination is shown to
Suha Mustafa Hassan +3 more
doaj +1 more source
Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 1, Page 85-93, January 2025.ABSTRACT Objective Accurate differentiation between placenta accreta spectrum (PAS) and uterine‐scar dehiscence with underlying non‐adherent placenta is often challenging, even for PAS experts, both prenatally and intraoperatively. We investigated the use of standardized two‐dimensional grayscale ultrasound and Doppler imaging markers in ...
T. Adu‐Bredu +3 more
wiley +1 more source
Zhongguo shiyan zhenduanxue, 2011 本文对我院产前诊断80例形态结构异常患儿病例进行回顾性分析,探讨三维超声在产前诊断胎儿形态结构异常中的临床价值。1资料与方法1 ...
张歆 +6 more
doaj
, 2002 【目的】探讨羊膜腔穿刺及脐带穿刺对高危妊娠结局的影响。【方法】对 160 例行羊膜腔穿刺及脐带穿刺的高危妊娠病例进行回 顾性分析。【结果】行产前诊断81 例,检出染色体异常 2 例,重型α或β 地中海贫血分别为 3 例及 1 例, B19 病毒感染合并胎儿畸形 1 例,均实 行了引产术,减少了严重先天缺陷儿的出生。羊水检查测定胎肺成熟度 79 例,适时终止妊娠, 减低了新生儿呼吸窘迫综合征的发生率。对羊 水过少及羊水过多试行了羊膜腔输液及放液治疗。无1 例因穿刺而发生感染、流产、早产者。【结论 ...
刘颖琳 +4 more
core