Lacerda L, Amaral O, Pinto R, Oliveira P, Aerts J, Sá Miranda M C
Unidade de Enzimologia, Instituto de Genética Médica Jacinto Magalhães, Porto, Portugal.
Clin Genet. 1994 Jun;45(6):298-300. doi: 10.1111/j.1399-0004.1994.tb04034.x.
In the Portuguese population the most frequent form of Gaucher disease is type 1. The N370S glucocerebrosidase gene mutation accounts for 63% of mutated alleles. The frequency of this mutation was accurately determined in the Portuguese population, which does not present an Ashkenazi Jewish genetic background. A gene frequency of 0.0043, with 95% confidence limits between 0.0023 and 0.0063, was obtained studying the genomic DNA of 2000 blood cards randomly sampled from the national neonatal screening program. On the basis of this frequency a significantly high number of homozygotes for the N370S mutation should be expected in the Portuguese population. This finding supports the idea that the majority of homozygotes for this mutation present a very mild clinical phenotype and remain undiagnosed.
在葡萄牙人群中,戈谢病最常见的类型是1型。N370S葡萄糖脑苷脂酶基因突变占突变等位基因的63%。该突变在葡萄牙人群中的频率已被精确测定,该人群没有阿什肯纳兹犹太遗传背景。通过研究从国家新生儿筛查项目中随机抽取的2000份血卡的基因组DNA,获得了基因频率为0.0043,95%置信区间在0.0023至0.0063之间。基于这一频率,预计葡萄牙人群中N370S突变的纯合子数量会显著增加。这一发现支持了这样一种观点,即该突变的大多数纯合子表现出非常轻微的临床表型,仍未被诊断出来。