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科威特的18三体综合征。

Trisomy 18 in Kuwait.

作者信息

Naguib K K, Al-Awadi S A, Moussa M A, Bastaki L, Gouda S, Redha M A, Mustafa F, Tayel S M, Abulhassan S A, Murthy D S

机构信息

Kuwait Medical Genetic Centre.

出版信息

Int J Epidemiol. 1999 Aug;28(4):711-6. doi: 10.1093/ije/28.4.711.

Abstract

BACKGROUND

Trisomy 18 (Edwards' syndrome, T18) is the second most common trisomy in man. We describe 118 children with regular T18 who were ascertained clinically and cytogenetically in the Kuwait Medical Genetics Centre during 1980-1997.

METHODS

Ascertainment of T18 cases was performed shortly after birth. Chromosomal studies were carried out in addition to other relevant investigations. To investigate the factors associated with T18, a case-control study was carried out with 131 normal healthy newborns. Studied factors included maternal and paternal age, birth order, abortion, associated malformation, and survival. Multiple logistic regression analysis was used to adjust for confounding between variables.

RESULTS

There was a preponderance of females among T18 cases (female:male ratio 2.1:1). The majority of T18 cases (53%) died before the second week of life. The most common associated anomalies were: congenital heart (38.1%) and gastrointestinal (25.4%). Multiplicity of malformations was also observed. Significant seasonal variation in T18 cases was detected with a peak in spring. Of the 118 T18 cases, 59 were delivered during 1994-1997 (average overall T18 birth prevalence rate 8.95 per 10 000 live births [95% CI: 6.66-11.23]). Concerning maternal age, 30.5% of the T18 cases' mothers were > or =35 years compared to 10.7% in the control group. The difference was statistically significant, P = 0.002. Logistic regression analysis showed that maternal age >30 years was a significant risk factor for T18, after adjusting for confounding with paternal age. Paternal age and abortion were not found to be significant risk factors.

CONCLUSION

Trisomy 18 birth prevalence rate is high in Kuwait with advanced maternal age as a significant risk factor.

摘要

背景

18三体综合征(爱德华兹综合征,T18)是人类第二常见的三体综合征。我们描述了1980年至1997年间在科威特医学遗传学中心通过临床和细胞遗传学确诊的118例典型T18患儿。

方法

T18病例在出生后不久确诊。除其他相关检查外,还进行了染色体研究。为了研究与T18相关的因素,对131例正常健康新生儿进行了病例对照研究。研究因素包括父母年龄、出生顺序、流产、相关畸形和存活情况。采用多元逻辑回归分析来调整变量之间的混杂因素。

结果

T18病例中女性占多数(女:男比例为2.1:1)。大多数T18病例(53%)在出生后第二周前死亡。最常见的相关畸形是:先天性心脏病(38.1%)和胃肠道畸形(25.4%)。还观察到畸形的多样性。检测到T18病例存在显著的季节性变化,春季达到高峰。在118例T18病例中,59例在1994年至1997年期间出生(T18总体平均出生患病率为每10000例活产8.95例[95%可信区间:6.66 - 11.23])。关于母亲年龄,T18病例的母亲中30.5%年龄≥35岁,而对照组为10.7%。差异具有统计学意义,P = 0.002。逻辑回归分析表明,在调整了父亲年龄的混杂因素后,母亲年龄>30岁是T18的一个显著危险因素。未发现父亲年龄和流产是显著的危险因素。

结论

科威特的18三体综合征出生患病率较高,母亲年龄较大是一个显著的危险因素。

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