本文選題：胎兒疾病 + 超聲檢查�。� 參考：《中國臨床醫(yī)學(xué)影像雜志》2015年08期

【摘要】：目的:評(píng)估孕中期超聲檢查對(duì)18-三體胎兒的診斷價(jià)值。方法:回顧分析本院13年間57例經(jīng)染色體核型分析確診為18-三體綜合征胎兒的聲像圖資料,探討對(duì)診斷該病有意義的聲像圖指標(biāo)。結(jié)果:聲像圖異常包括室間隔缺損、脈絡(luò)叢囊腫、宮內(nèi)生長(zhǎng)受限、重疊指、草莓頭、單臍動(dòng)脈、足畸形、羊水過多、小腦發(fā)育不良、耳位低置、小下頜和鼻骨發(fā)育不良,分別占46%、44%、42%、40%、33%、33%、26%、23%、21%、16%、12%、11%。聲像圖異常占89%,82%的胎兒均表現(xiàn)為2種及2種以上異常指標(biāo)。結(jié)論:孕中期超聲檢查對(duì)診斷18-三體綜合征具有一定的意義,結(jié)合染色體核型分析可提高18-三體綜合征的產(chǎn)前診斷率,并能降低出生率。
[Abstract]:Objective: To evaluate the diagnostic value of medium-term ultrasonography in the diagnosis of 18- triplet fetus. Methods: To review and analyze the ultrasonographic data of 57 cases of the fetus diagnosed by chromosome karyotype analysis in 13 years in our hospital, and to explore the significance of the sound image index for the diagnosis of the disease. Restriction of growth, overlapping finger, strawberry head, single umbilical artery, foot deformity, amniotic fluid, cerebellum dysplasia, low ear position, small mandibular and nasal bone dysplasia, accounted for 46%, 44%, 42%, 40%, 33%, 33%, 26%, 23%, 21%, 16%, 12%, abnormal 11%. of 89%. The diagnosis of 18- trisomy syndrome has certain significance. Combined with chromosome karyotype analysis, the prenatal diagnosis rate of 18- trisomy syndrome can be increased, and the birth rate can also be reduced.
【作者單位】： 深圳市人民醫(yī)院;深圳市坪山新區(qū)人民醫(yī)院中心實(shí)驗(yàn)室;
【基金】：深圳市科技創(chuàng)新委員會(huì)項(xiàng)目(JCYJ20130401093116730) 廣東省科技計(jì)劃項(xiàng)目(2013B060400011)
【分類號(hào)】：R714.5;R445.1

【參考文獻(xiàn)】

中國期刊全文數(shù)據(jù)庫 前1條

1 栗河舟;王銘;許雅娟;吳sダ，

本文編號(hào)：2112118