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首页> 外文期刊>Brain: A journal of neurology >Minimum birth prevalence of mitochondrial respiratory chain disorders in children.
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Minimum birth prevalence of mitochondrial respiratory chain disorders in children.

机译:儿童线粒体呼吸链疾病的最低出生率。

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Mitochondrial respiratory chain disorders comprise a group of perhaps several hundred different genetic diseases. Each individual disorder is rare, but collectively they account for substantial use of health care resources. However, few accurate data on prevalence are available due to problems such as variation in clinical presentation, age of onset, referral practices and limitations of diagnostic methodologies. With this retrospective study, we aimed to determine the minimum birth prevalence of respiratory chain disorders that have onset in childhood, that is the proportion of births that will have onset of symptoms caused by a respiratory chain defect by 16 years of age. Of the 1 706 694 children born in the three south-eastern states of Australia (New South Wales, Victoria and South Australia) between January 1st 1987 and December 31st 1996, samples from 430 were referred for investigation of a respiratory chain disorder. Definite diagnosis of a respiratory chain disorder was made in 86 cases basedon defined clinical, pathological, enzyme and molecular criteria. Age at presentation ranged from 0 to 129 months (median 4 months). The total data set predicts a minimum birth prevalence for respiratory chain disorders in children of 5.0/100 000 [95% confidence interval (CI) 4.0-6.2]. A significantly higher figure of 58.6/100 000 (95% CI 34.7-92.6) was noted for Australian families of Lebanese origin. Clinical awareness of respiratory chain disorders and investigation methods have improved since 1987, but not all affected children would have been recognized as such from the more recent years. The minimum birth prevalence of 6.2/100 000 (95% CI 4.5-8.4) for the 43 patients born between 1991 and 1994 is thought to be a more accurate estimate for respiratory chain disorders presenting in childhood. Combining our data with a previous study on prevalence of adult-onset respiratory chain disorders predicts a minimum birth prevalence of 13.1/100 000 or 1/7634 for respiratory chain disorders with onset at any age.
机译:线粒体呼吸链疾病包括一组可能数百种不同的遗传疾病。每种疾病都很罕见,但总的来说,它们占了医疗资源的大量使用。然而,由于诸如临床表现的变化,发病年龄,转诊实践和诊断方法的局限性等问题,几乎没有关于患病率的准确数据。通过这项回顾性研究,我们旨在确定儿童期开始的呼吸链疾病的最低出生流行率,即到16岁时会出现由呼吸链缺陷引起的症状的出生比例。在1987年1月1日至1996年12月31日期间,在澳大利亚的三个东南部州(新南威尔士州,维多利亚州和南澳大利亚州)出生的1 706 694名儿童中,有430名样本被送去调查呼吸链疾病。根据明确的临床,病理,酶和分子标准,对86例患者进行了呼吸链疾病的明确诊断。报告时的年龄为0到129个月(中位数为4个月)。总数据集预测,儿童呼吸链疾病的最低出生患病率为5.0 / 100 000 [95%置信区间(CI)4.0-6.2]。澳大利亚黎巴嫩裔家庭的数字显着更高,为58.6 / 100 000(95%CI 34.7-92.6)。自1987年以来,人们对呼吸链疾病和调查方法的临床认识已有所提高,但从最近几年开始,并不是所有受影响的儿童都已意识到这一点。 1991年至1994年之间出生的43例患者的最低出生患病率是6.2 / 100 000(95%CI 4.5-8.4),这是对儿童时期出现的呼吸链疾病的更准确估计。将我们的数据与以前关于成人发作性呼吸链疾病患病率的研究相结合,可以预测任何年龄段发作的呼吸链疾病的最低出生患病率分别为13.1 / 10万或1/7634。

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