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全球范围内针对因21-羟化酶缺乏所致经典型先天性肾上腺皮质增生症的新生儿筛查经验。

Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

作者信息

Pang S Y, Wallace M A, Hofman L, Thuline H C, Dorche C, Lyon I C, Dobbins R H, Kling S, Fujieda K, Suwa S

机构信息

Department of Pediatrics, University of Illinois, College of Medicine, Chicago 60612.

出版信息

Pediatrics. 1988 Jun;81(6):866-74.

PMID:3259306
Abstract

The need for a reliable screening test for classical congenital adrenal hyperplasia prompted development of newborn screening programs. Worldwide incidence of classical congenital adrenal hyperplasia in this report was taken from newborn screening programs in France, Italy, Japan, New Zealand, Scotland, and the United States. Two populations in which the occurrence of congenital adrenal hyperplasia among live births has been reported with greater than usual frequency are the Yupik Eskimos of southwestern Alaska (1:282) and the people of La Reunion, France (1:2,141). Aside from these populations, 1,093,310 newborns were screened between 1980 and 1988, of whom 77 had congenital adrenal hyperplasia. Thus, worldwide incidence of this disorder was estimated at 1:14,199 live births for homozygous patients, 1:60 for heterozygous subjects, with a gene frequency of 0.0083. Incidence of congenital adrenal hyperplasia among whites was estimated to be 1:11,909 (41:488,279) for homozygous patients, 1:55 for heterozygous subjects with a gene frequency of 0.0091. Incidence for the salt-wasting form of congenital adrenal hyperplasia was 1:18,850 (58:1,093,310) compared with 1:57,543 (19:1,093,310) for congenital adrenal hyperplasia in the simple virilizing form. Thus, salt-wasting congenital adrenal hyperplasia was three times more common than simple virilizing congenital adrenal hyperplasia. Estimated incidence of congenital adrenal hyperplasia in white populations in Italy and France (1:10,866) was higher than in Scotland (1:17,098), New Zealand (1:14,500). The incidence in an Asian population (Japan) (1:15,800) did not differ significantly from that of the white population. In four of five populations, overall incidence was higher than previously reported, as was the frequency of the salt-wasting form (75% v 50% to 66%), suggesting improved case detection by newborn screening.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对经典型先天性肾上腺皮质增生症进行可靠筛查测试的需求促使了新生儿筛查项目的开展。本报告中经典型先天性肾上腺皮质增生症的全球发病率取自法国、意大利、日本、新西兰、苏格兰和美国的新生儿筛查项目。据报道,阿拉斯加西南部的尤皮克爱斯基摩人(1:282)和法国留尼汪岛的居民(1:2,141)这两个人群中,活产儿中先天性肾上腺皮质增生症的发病率高于正常频率。除了这些人群外,1980年至1988年间对1,093,310名新生儿进行了筛查,其中77人患有先天性肾上腺皮质增生症。因此,该疾病的全球发病率估计为纯合子患者每14,199例活产中有1例,杂合子个体每60例中有1例,基因频率为0.0083。白人中先天性肾上腺皮质增生症的发病率估计为纯合子患者每11,909例中有1例(41:488,279),杂合子个体每55例中有1例,基因频率为0.0091。失盐型先天性肾上腺皮质增生症的发病率为1:18,850(58:1,093,310),而单纯男性化型先天性肾上腺皮质增生症的发病率为1:57,543(19:1,093,310)。因此,失盐型先天性肾上腺皮质增生症比单纯男性化型先天性肾上腺皮质增生症常见三倍。意大利和法国白人人群中先天性肾上腺皮质增生症的估计发病率(1:10,866)高于苏格兰(1:17,098)、新西兰(1:14,500)。亚洲人群(日本)的发病率(1:15,800)与白人人群无显著差异。在五个人群中的四个中,总体发病率高于先前报道,失盐型的频率也是如此(75%对50%至66%),这表明通过新生儿筛查病例发现有所改善。(摘要截取自250字)

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