1975-1984年修订的匈牙利人口资料中不同先天性肢体缺陷类型的出生患病率

Acta morphologica Hungarica Pub Date : 1991-01-01
A Czeizel, M Vitéz, I Kodaj, W Lenz
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引用次数: 0

摘要

1975-1984年,匈牙利对998例肢体复位缺陷患者进行了评估。通过对其他确定来源的检查,匈牙利先天性异常登记处的完成率为98.4%。误诊率为12.6%。在本研究所涵盖的期间,患有先天性肢体缺损的修订病例的出生流行率为每1000名新生儿中0.55人。孤立病例与多发病例分离。修订后孤立病例的出生患病率为0.35‰。根据表型表现将其分为6型。由于不同类型先天性肢体缺陷的患肢数量、单发与多发比例、性别比例存在明显差异,故应分别评估其病因。
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Birth prevalence of different congenital limb deficiency types in a revised, population based Hungarian material, 1975-1984.

998 cases affected with limb reduction deficiency were evaluated in Hungary, 1975-1984. Through the check-up of other sources of ascertainments, the Hungarian Congenital Abnormality Registry was found to be 98.4% complete. The proportion of misdiagnoses was 12.6%. In the period encompassed by the study, the birth prevalence of revised cases affected with congenital limb reduction deficiency was 0.55 per 1000 total births. Isolated and multiple cases were separated. The birth prevalence of revised isolated cases was 0.35 per 1000. Six types were separated based on their phenotypic manifestations. As the number of affected limbs, ratio of isolated and multiple cases and sex ratio showed obvious differences, etiological factors should be evaluated separately in these different types of congenital limb deficiencies.

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Electrical Signs of Activity in Assemblies of Neurons: Compound Field Potentials as Objects of Study in Their Own Right Influence of chromatin condensation on the absorption spectra of nuclei stained with toluidine blue. A new computerized polarization--microscopic method for the demonstration of collagen fibers. Generalized secondary amyloidosis in rheumatoid arthritis. Etiological study on isolated proximal intercalary type of congenital limb deficiency in Hungary, 1975-1984.
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