Barlow-Stewart Kristine, Gaff Clara, Emery Jon, Metcalfe Sylvia A
The Centre for Genetics Education of NSW Health, Faculty of Medicine, Sydney, New South Wales.
Aust Fam Physician. 2007 Oct;36(10):802-5.
A comprehensive family history, regularly updated and including the patient's ancestry and cultural background can aid in diagnosis, risk prediction, referral and genetic testing.
This article discusses the professional and support services available to families following the identification of a genetic condition or mutated gene, conferring individual or reproductive risk.
Genetic testing for a range of conditions is available for diagnostic, carrier, predictive and presymptomatic purposes. Genetic testing for ancestry promoted widely on the internet has little or no scientific validity. Patients should be strongly encouraged to share their genetic information to enable cascade genetic testing. Genetics services provide current information, and where appropriate, discussion of reproductive options and genetic testing after consideration of all the implications and support for the decision making and its consequences engendered. Support groups for specific conditions are important partners in the provision of support for families with genetic conditions.
一份全面的家族病史,定期更新并包含患者的祖籍和文化背景,有助于诊断、风险预测、转诊和基因检测。
本文讨论了在确定遗传疾病或突变基因后,为家庭提供的专业和支持服务,这些疾病会带来个人或生殖风险。
针对一系列疾病的基因检测可用于诊断、携带者检测、预测和症状前检测。在互联网上广泛推广的祖籍基因检测几乎没有科学依据。应大力鼓励患者分享他们的基因信息,以便进行级联基因检测。遗传学服务提供最新信息,并在适当情况下,在考虑所有影响因素后,讨论生殖选择和基因检测,为决策及其后果提供支持。针对特定疾病的支持小组是为患有遗传疾病的家庭提供支持的重要合作伙伴。