葡萄牙眼科学会和葡萄牙人类遗传学学会遗传性视网膜营养不良基因检测联合临床实践指南。

IF 2.9 3区 医学 Q2 GENETICS & HEREDITY Clinical Genetics Pub Date : 2025-01-02 DOI:10.1111/cge.14691
João Pedro Marques, Célia Azevedo Soares, Ana Luísa Carvalho, Sérgio Estrela-Silva, Luísa Coutinho Santos, Lina Ramos, Eduardo Silva
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引用次数: 0

摘要

葡萄牙眼科学会和葡萄牙人类遗传学学会制定了临床实践指南,以简化遗传性视网膜营养不良症(IRDs)的基因检测,强调分子诊断在加强患者护理方面的关键作用。基因检测在诊断、遗传咨询、预后和获得临床试验以及新的基因特异性治疗方面至关重要。这些指南建议对所有IRD患者进行基因检测,并提供了对现有检测方法的详细评估,确保将遗传咨询纳入眼科护理。这一过程的关键是包括至少一次遗传咨询会议,以便与患者和家属/护理人员有效沟通和讨论检测结果的影响。主要建议包括级联检测,以确定有风险的家庭成员,并根据国际标准对变异分类进行标准化,以确保诊断和护理的一致性。眼科随访时间一般为成人1-2年,儿科患者6个月,以监测疾病进展和并发症。讨论了儿科方面的考虑,反映了与检测未成年人有关的复杂性和伦理问题。这些指南旨在提高诊断准确性,指导治疗决策并最终改善患者预后,标志着ird遗传管理的重大进展。
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Portuguese Society of Ophthalmology and Portuguese Society of Human Genetics Joint Clinical Practice Guidelines for Genetic Testing in Inherited Retinal Dystrophies.

The Portuguese Society of Ophthalmology and the Portuguese Society of Human Genetics developed clinical practice guidelines to streamline genetic testing for inherited retinal dystrophies (IRDs), underlining the critical role of molecular diagnosis in enhancing patient care. Genetic testing is pivotal in diagnosis, genetic counselling, prognosis and access to clinical trials, and new gene-specific therapies. These guidelines recommend genetic testing in all IRD patients and provide a detailed assessment of available testing methods, ensuring that genetic counselling is integrated into ophthalmic care. Essential to this process is the inclusion of at least one genetic counselling session to effectively communicate and discuss implications of test results with patients and families/carers. Key recommendations include cascade testing to identify at-risk family members and standardisation of variant classification according to international criteria to ensure consistency in diagnosis and care. Ophthalmological follow-up is generally prescribed at intervals of 1-2 years for adults and 6 months for paediatric patients, to monitor disease progression and complications. Paediatric considerations are addressed, reflecting the complexities and ethical concerns associated with testing minors. These guidelines aim to elevate diagnostic accuracy, guide therapeutic decisions and ultimately improve patient outcomes, marking a significant advance in the genetic management of IRDs.

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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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