打印 妙佑医疗国际的方法 团队合作。 妙佑医疗国际临床基因组学科室的医学遗传学家、经认证的遗传咨询师与其他所需专业人员通力合作评估各类遗传性医学状况,协调各种检测和手术。 综合服务。 临床基因组学科室提供罕见、遗传疾病的诊断性检查和遗传性癌症综合征的遗传学评估、对患者和家属进行全面的家族史调查、对患者和家属进行家族性疾病教育,并为家庭成员提供咨询服务,从而促进其对遗传病影响的理解。 先进技术。 临床基因组学科室在医学上适当的范围内,根据具体情况提供最新基因检测技术。 研究。 妙佑医疗国际因其在遗传学和基因组学研究方面的卓越贡献而闻名。患者有机会参加基因研究,从而改善其整体护理。妙佑医疗国际个体化医学中心致力于将最新科技进步与临床护理相结合。 在妙佑医疗国际的体验与患者故事 患者告诉我们,互动质量、关注细节以及就医效率都是他们从未经历过的医疗体验。查看妙佑医疗国际满意患者的故事。 Genetic testing reveals cause of patient's mysterious lifelong illnessAndy Grundstad was sick and tired of feeling sick and tired. "I felt like I was 80 years old," says Andy, a 35-year-old agronomist living outside of Crosby, North Dakota. He'd been diagnosed with vasculitis as a child and lived with various health issues while care teams struggled to provide a comprehensive diagnosis and effective treatment. Andy's symptoms worsened after a stroke in 2017. Near-daily fevers and joint pain accompanied a second stroke in 2020.… 专长与排名 美国首家为患者提供淋巴瘤基因组诊断检测的机构。 妙佑医疗国际开发了一种检测方法,可为弥漫性大 B 细胞淋巴瘤(最常见的非霍奇金淋巴瘤)患者的诊断和治疗提供帮助。 全美公认的专业实力。 妙佑医疗国际的临床基因组学科室拥有取得专科认证的资深医学遗传学家和经认证的遗传咨询师。拥有一支综合性的团队,可以为所有年龄段、病情复杂度各不相同的人群提供服务,根据每个人的需求量身定制治疗方案。 前沿研究。 妙佑医疗国际的临床基因组学科室因其在研究方面的杰出贡献受到业内的广泛认可,同时还拥有关于罕见或新型遗传病长期发表研究的丰富经验。 妙佑医疗国际儿童中心 技术精湛的儿科专家针对所有类型的儿童状况提供诊断和治疗。我们以团队的形式,携手寻找答案和设定目标,并根据孩子的不同需求来制定治疗计划。 详细了解儿童中心。 位置、旅行和住宿Mayo Clinic 在亚利桑那州的芬尼克斯和斯克茨戴尔、佛罗里达州的杰克逊威尔和明尼苏达州的罗切斯特都有主要校区。Mayo Clinic 健康系统在几个州拥有十几个工作地点。 有关参观 Mayo Clinic 的更多信息,请在下面选择您的位置: 妙佑医疗国际亚利桑那州院区 妙佑医疗国际佛罗里达州院区 妙佑医疗国际明尼苏达州院区 妙佑区域医疗系统 伦敦妙佑医疗中心 费用与保险妙佑医疗国际与数百家保险公司合作,是数百万人的网络内医疗服务提供者。 在大多数情况下,妙佑医疗国际不需要医生转诊。某些保险公司要求转诊,或有其他特定医疗要求。所有约诊的优先级都以医疗需求为基础。 详细了解在妙佑医疗国际约诊的信息。 请联系您的保险公司,核实承保范围,并在就医之前获得任何所需的授权。保险公司的客户服务号码通常印在保险卡背面。 有关账单与保险的更多信息: 妙佑医疗国际设于亚利桑那州、佛罗里达州以及明尼苏达州的院区 妙佑区域医疗系统 临床试验 探索 Mayo Clinic 的研究 测试新的治疗、干预与检查方法,旨在预防、检测、治疗或控制这种疾病。 来自妙佑医疗国际员工 申请预约 医生与科室 July 02, 2022 打印 显示参考文献 National Library of Medicine. Help me understand genetics. Genetics Home Reference. https://ghr.nlm.nih.gov/primer. Accessed Feb. 13, 2017. Frequently asked questions about genetic testing. National Human Genome Research Institute. https://www.genome.gov/19516567/faq-about-genetic-testing/. Accessed Feb. 13, 2017. Genetic testing for hereditary cancer syndromes. National Cancer Institute. https://www.cancer.gov/about-cancer/causes-prevention/genetics/genetic-testing-fact-sheet. Accessed Feb. 13, 2017. Raby BA, et al. Genetic testing. http://www.uptodate.com/home. Accessed Feb. 13, 2017. Grody WW, et al. ACMG position statement on prenatal/preconception expanded carrier screening. Genetics in Medicine. 2013;15:482. Genetic testing. American Medical Association. https://www.ama-assn.org/content/genetic-testing. Accessed Feb. 13, 2017. Frequently asked questions. Prenatal genetic diagnostic tests. FAQ164. Pregnancy. American College of Obstetricians and Gynecologists. https://www.acog.org/-/media/For-Patients/faq164.pdf?dmc=1&ts=20161216T1208042192. Accessed Feb. 13, 2017. Breast cancer risk factors you cannot change. American Cancer Society. https://www.cancer.org/cancer/breast-cancer/risk-and-prevention/breast-cancer-risk-factors-you-cannot-change.html. Accessed Feb. 21, 2017. Medical review (expert opinion). Mayo Clinic, Jacksonville, Fla. Feb. 24, 2017. 相关 三 X 染色体综合征 不孕不育症 乳腺癌基因检测 亨廷顿病 侏儒症 先天性睾丸发育不全综合征 先天性肾上腺皮质增生症 共济失调 凝血因子 V 莱顿突变 副神经节瘤 努南综合征 原发性进行性失语症 唐氏综合征 嗜铬细胞瘤 囊性纤维化 地中海贫血 埃勒斯-当洛斯综合征 大疱性表皮松解症 威尔逊氏症 安格尔曼综合征 少精子症 尿崩症 布鲁加达综合征 戈谢病 扩张型心肌病 早老症 普拉德-威利综合征 林奇综合征 流产后怀孕 海绵状血管畸形 特纳综合征 男性不育症 男性性腺功能减退症 真性红细胞增多症 神经鞘瘤病 结肠息肉 绘制基因组信息 肌营养不良 肥厚型心肌病 肺高压 胸主动脉瘤 脉络丛癌 脑瘫 腓骨肌萎缩症 苯丙酮尿症(PKU) 血色素沉着症 视频:绒毛活检 迪格奥尔格综合征(22q11.2 缺失综合征) 遗传学与心肌病 长 QT 综合征 雷特综合征 非典型生殖器 颅缝早闭 马方综合征 骨髓纤维化 显示更多相关内容 Mayo Clinic 新闻 (VIDEO) From 125 fractures to the front lines of discovery: A Mayo Clinic resident's unbreakable journey May 22, 2025, 11:00 a.m. CDT Hidden mutation leads to groundbreaking genetic discovery April 03, 2025, 12:00 p.m. CDT Mayo Clinic researchers identify a measurable genetic mutation as a significant predictor of metastasis and survival in pancreatic cancer March 19, 2025, 05:03 p.m. CDT Researchers resolve uncertainty in BRCA2 testing, improving cancer risk assessment and patient care Jan. 08, 2025, 05:01 p.m. CDT 10 pioneering studies from Mayo Clinic's Center for Individualized Medicine in 2024 Dec. 23, 2024, 03:00 p.m. CDT Addressing the root cause of rare diseases -- the promise of antisense oligonucleotides Dec. 19, 2024, 04:00 p.m. CDT What's your health forecast? 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