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首页> 外文期刊>Paediatric and perinatal epidemiology >A population-based study of the recurrence of developmental disabilities--Metropolitan Atlanta Developmental Disabilities Surveillance Program, 1991-94.
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A population-based study of the recurrence of developmental disabilities--Metropolitan Atlanta Developmental Disabilities Surveillance Program, 1991-94.

机译:基于人群的发展性残疾复发的研究-大都会亚特兰大发展性残疾监测计划,1991-94年。

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Serious developmental disabilities (DD) are quite common and affect approximately 2% of all school-aged children. The impact of DDs with respect to the need for special education services, medical care and the demand on family members can be enormous. While this impact can be magnified for families with more than one child with a DD, little is known regarding the epidemiology of recurrence of DDs. When the cause of a DD is unknown, genetic counsellors rely on recurrence risk estimates which for DDs are over 10 years old. The objectives of our study were to: (1) assess the contribution of recurrent cases to the prevalence of DDs; (2) provide current, population-based recurrence risk estimates; and (3) examine characteristics of the first affected child as predictors of recurrence. Two population-based data sources were used to identify all children born to the same mother during the period 1981-91 in the five-county metropolitan Atlanta area with at least one of four DDs: mental retardation (MR), cerebral palsy, hearing loss, or vision impairment. Recurrence risk estimates for these DDs ranged from 3% to 7% and were many times higher than the background prevalences. The risk of recurrence of DDs was greatest for MR - approximately eight times greater than the baseline MR prevalence. Isolated mild MR (IQ 50-70) was highly concordant between siblings with MR. Sex, race, and birthweight of the index child, maternal education, and maternal age were not significantly associated with recurrence risk. Further research is needed to investigate the roles of genetic and environmental factors on the recurrence of DDs, particularly isolated mild MR.
机译:严重的发育障碍(DD)很常见,约占所有学龄儿童的2%。 DD对特殊教育服务,医疗保健和家庭成员需求的影响可能是巨大的。虽然对于有一个以上DD儿童的家庭来说,这种影响可以被放大,但对于DD复发的流行病学知之甚少。当DD的原因未知时,遗传咨询师将依赖于DD超过10年的复发风险估计。我们研究的目的是:(1)评估复发病例对DD患病率的影响; (2)提供基于人群的当前复发风险评估; (3)检查第一个患病儿童的特征作为复发的预测因子。使用两个基于人口的数据源来识别1981-91年间在五县城亚特兰大地区同一母亲所生的所有孩子,其中至少四个DD之一:智力低下(MR),脑瘫,听力下降或视力障碍。这些DD的复发风险估计范围为3%至7%,比背景患病率高出许多倍。 DD复发的风险对于MR来说最大,大约是基线MR患病率的八倍。孤立的轻度MR(IQ 50-70)与MR的兄弟姐妹之间高度一致。索引儿童的性别,种族和出生体重,母亲的教育程度和母亲的年龄与复发风险没有显着相关。需要进一步的研究来调查遗传因素和环境因素在DDs,特别是轻度MR复发中的作用。

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