帕金森病
肌张力障碍
队列
人口
医学
遗传异质性
GTP环水解酶I
遗传学
儿科
精神科
内科学
疾病
表型
生物
基因
四氢生物蝶呤
环境卫生
一氧化氮
一氧化氮合酶
作者
Valerija Dobričić,Aleksandra Tomić,V. Branković,Nikola Kresojević,Milena Janković,Ana Westenberger,Vedrana Milić Rašić,Christine Klein,Ivana Novaković,Marina Svetel,Vladimir Kostić
标识
DOI:10.1016/j.parkreldis.2017.09.017
摘要
GTP cyclohydrolase 1-deficient DOPA-responsive dystonia, caused by autosomal dominant mutation in the gene coding for GTP cyclohydrolase 1, is a rare disorder with a reported prevalence of 0.5 per million. A correct diagnosis of DRD is crucial, given that this is an exquisitely treatable neurogenetic disorder. Although genetic testing is now widely available, we hypothesize that DRD is still underdiagnosed and its prevalence underestimated.Molecular genetic analysis of the GCH1 gene was performed in a representative cohort of 47 Serbian patients with clinical features of DRD and in their 16 available relatives. The DRD prevalence rate in Serbia was estimated based on population size, catchment area, and the centralized Serbian referral system for rare diseases.We identified 9 different GCH1 mutations in 23 individuals from 11 families, 5 of which are novel. Patients displayed a broad range of clinical phenotypes. The estimated prevalence of GCH1-related DOPA-responsive dystonia in Serbia was 2.96 per million individuals and there was no evidence for a common founder.Our data expand the genotypic spectrum of GCH1 and confirm the broad phenotypic spectrum of DRD in the Serbian population. The number of detected mutation carriers in this sample implies that the frequency of DRD in the Serbian population is considerably higher than expected based on published prevalence rates, suggesting that the prevalence of this treatable disease should be revisited also in other populations.
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