Coto E, Bousoño C, Menéndez M J, Cue R, Toral J F, Benavides A, Hernando I, Plasencia A, López-Larrea C
Laboratorio de Genética Molecular (Servicio de Inmunología), Hospital Central Universitario de Asturias, Oviedo.
Med Clin (Barc). 1994 Nov 26;103(18):681-3.
Cystic fibrosis (CF) is the most common autosomic-recessive inherited disorder. More than 300 different mutations in the CF gene (CFTR) have been described, being delta F508 and G542X the most common in the Spanish population. The frequencies of these mutations vary between the different European populations.
We have studied the delta F508 and G542X mutations in 20 CF-patients from Asturias. These mutations were analysed through the polymerase chain reaction (PCR).
The frequency of the delta F508 mutation in Asturias was 77.5%, higher than those found in most of the other Spanish populations. The frequency found in Asturias is close to the frequency described for the Basque Country population. Patients homozygous for the delta F508 mutation showed clinical symptoms similar to those described in studies on other populations.
The high frequency of two mutations in the CFTR gene in Asturias makes possible the direct diagnostic in most families. The delta F508 mutation is associated to severe clinical manifestations, like early pancreatic insufficiency and Pseudomonas infection.
囊性纤维化(CF)是最常见的常染色体隐性遗传性疾病。CF基因(CFTR)中已发现300多种不同的突变,其中ΔF508和G542X在西班牙人群中最为常见。这些突变在不同欧洲人群中的频率有所不同。
我们研究了来自阿斯图里亚斯的20例CF患者中的ΔF508和G542X突变。通过聚合酶链反应(PCR)分析这些突变。
阿斯图里亚斯地区ΔF508突变的频率为77.5%,高于大多数其他西班牙人群。阿斯图里亚斯地区发现的频率与巴斯克地区人群所描述的频率相近。ΔF508突变纯合子患者表现出与其他人群研究中描述的类似临床症状。
阿斯图里亚斯地区CFTR基因中两种突变的高频率使得大多数家庭能够进行直接诊断。ΔF508突变与严重的临床表现相关,如早期胰腺功能不全和铜绿假单胞菌感染。