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Genetic Counseling in Huntingtons Disease: Potential New Challenges on Horizon?

机译:亨廷顿氏病的遗传咨询:地平线潜在的新挑战?

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摘要

Huntington's disease (HD) is a rare, hereditary, neurodegenerative and dominantly transmitted disorder affecting about 10 out of 100,000 people in Western Countries. The genetic cause is a CAG repeat expansion in the huntingtin gene (HTT), which is unstable and may further increase its length in subsequent generations, so called anticipation. Mutation repeat length coupled with other gene modifiers and environmental factors contribute to the age at onset in the offspring. Considering the unpredictability of age at onset and of clinical prognosis in HD, the accurate interpretation, a proper psychological support and a scientifically sound and compassionate communication of the genetic test result are crucial in the context of Good Clinical Practice and when considering further potential disease-modifying therapies. We discuss various genetic test scenarios that require a particularly careful attention in psychological and genetic counseling and expect that the counseling procedures will require a constant update.
机译:亨廷顿舞蹈病(HD)是一种罕见的遗传性,神经退行性疾病和主要传播性疾病,在西方国家的100,000人中约有10人受到影响。遗传原因是亨廷顿基因(HTT)中的CAG重复扩增,这是不稳定的,并可能在后代中进一步增加其长度,即所谓的预期。突变的重复长度与其他基因修饰子和环境因素一起导致了后代发病年龄的增加。考虑到HD患者起病年龄和临床预后的不可预测性,对于良好的临床实践以及在考虑进一步的潜在疾病时,准确的解释,适当的心理支持以及基因检测结果的科学合理和富有同情心的交流至关重要。修改疗法。我们讨论了各种基因测试方案,这些方案在心理和遗传咨询中需要特别注意,并期望咨询程序将需要不断更新。

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