从婴儿期到青春期遗传性帕金森病的临床和神经影像学表型。

Hugo Morales‐Briceño, S. Mohammad, B. Post, A. Fois, R. Dale, M. Tchan, V. Fung
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引用次数: 22

摘要

遗传性早发性帕金森病表现于婴儿期至青春期(≤21岁),是一种临床多样化的综合征,常合并其他多动运动障碍、神经和影像学异常。这种综合征在基因上是异质的,有许多致病基因已经为人所知。随着新一代测序在临床实践中的使用增加,对表型-基因型相关性和新的致病基因的发现有了新的和意想不到的见解。现在人们认识到,单个基因的突变可以产生广泛的表型谱,相反,不同的遗传疾病可以表现为相似的表型。准确的表型表征仍然是解释未确诊患者遗传发现的重要步骤。然而,在过去的十年中,关于致病基因的数量和早发病例的表型谱的知识有了显著的扩展。对遗传疾病及其临床表现的详细了解是合理规划基因和分子检测以及正确解释下一代测序结果的必要条件。在这篇综述中,我们研究了发病≤21年的遗传性帕金森病的相关文献,提取了相关运动障碍以及其他神经学和影像学特征的数据,以描述与早发性帕金森病相关的综合征模式。排除PRKN (parkin)突变,>90%的呈现表型具有复杂或非典型的表现,其中肌张力障碍、异常认知、锥体体征、神经精神障碍、异常成像和异常眼动是最常见的特征。此外,一些影像学特征和神经外表现对某些疾病是相对特异性的,是重要的诊断线索。从目前可用的文献来看,早发性帕金森病最常见的原因已经阐明,但在许多情况下诊断仍然具有挑战性。大约70种不同基因的突变与早发性帕金森病有关,或者可能将帕金森病作为其表型谱的一部分。大多数病例由隐性遗传突变引起,其次是显性和x连锁突变,很少由线粒体遗传突变引起。在婴儿期帕金森氏症中,低运动刚性综合征的表型最常由单胺合成障碍引起。在儿童期和青少年发病病例中,常见的基因型包括PRKN、HTT、ATP13A2、ATP1A3、FBX07、PINK1和PLA2G6突变。此外,威尔逊氏病和锰转运体突变是潜在的可治疗的疾病,在任何早发性帕金森病患者的鉴别诊断中都应考虑到这一点。
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Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence.
Genetic early-onset parkinsonism presenting from infancy to adolescence (≤21 years old) is a clinically diverse syndrome often combined with other hyperkinetic movement disorders, neurological and imaging abnormalities. The syndrome is genetically heterogeneous, with many causative genes already known. With the increased use of next-generation sequencing in clinical practice, there have been novel and unexpected insights into phenotype-genotype correlations and the discovery of new disease-causing genes. It is now recognized that mutations in a single gene can give rise to a broad phenotypic spectrum and that, conversely different genetic disorders can manifest with a similar phenotype. Accurate phenotypic characterization remains an essential step in interpreting genetic findings in undiagnosed patients. However, in the past decade, there has been a marked expansion in knowledge about the number of both disease-causing genes and phenotypic spectrum of early-onset cases. Detailed knowledge of genetic disorders and their clinical expression is required for rational planning of genetic and molecular testing, as well as correct interpretation of next-generation sequencing results. In this review we examine the relevant literature of genetic parkinsonism with ≤21 years onset, extracting data on associated movement disorders as well as other neurological and imaging features, to delineate syndromic patterns associated with early-onset parkinsonism. Excluding PRKN (parkin) mutations, >90% of the presenting phenotypes have a complex or atypical presentation, with dystonia, abnormal cognition, pyramidal signs, neuropsychiatric disorders, abnormal imaging and abnormal eye movements being the most common features. Furthermore, several imaging features and extraneurological manifestations are relatively specific for certain disorders and are important diagnostic clues. From the currently available literature, the most commonly implicated causes of early-onset parkinsonism have been elucidated but diagnosis is still challenging in many cases. Mutations in ∼70 different genes have been associated with early-onset parkinsonism or may feature parkinsonism as part of their phenotypic spectrum. Most of the cases are caused by recessively inherited mutations, followed by dominant and X-linked mutations, and rarely by mitochondrially inherited mutations. In infantile-onset parkinsonism, the phenotype of hypokinetic-rigid syndrome is most commonly caused by disorders of monoamine synthesis. In childhood and juvenile-onset cases, common genotypes include PRKN, HTT, ATP13A2, ATP1A3, FBX07, PINK1 and PLA2G6 mutations. Moreover, Wilson's disease and mutations in the manganese transporter are potentially treatable conditions and should always be considered in the differential diagnosis in any patient with early-onset parkinsonism.
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