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新型多学科眼科遗传学临床设计及成果。

Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic.

机构信息

University of Michigan Medical School, Ann Arbor, MI 48109, USA.

Kellogg Eye Center, Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA.

出版信息

Genes (Basel). 2023 Mar 15;14(3):726. doi: 10.3390/genes14030726.

Abstract

The Multidisciplinary Ophthalmic Genetics Clinic (MOGC) at the University of Michigan Kellogg Eye Center aims to provide medical and ophthalmic genetics care to patients with inherited ocular conditions. We have developed a clinical and referral workflow where each patient undergoes coordinated evaluation by our multidisciplinary team followed by discussions on diagnosis, prognosis, and genetic testing. Testing approaches are specific to each patient and can be targeted (single-gene, gene panel), broad (chromosomal microarray, whole-exome sequencing), or a combination. We hypothesize that this clinic model improves patient outcomes and quality of care. A retrospective chart review of patients in the MOGC from July 2020 to October 2022 revealed that the most common referral diagnoses were congenital cataracts, optic neuropathy, and microphthalmia, with 52% syndromic cases. Within this patient cohort, we saw a 76% uptake for genetic testing, among which 33% received a diagnostic test result. Our results support a tailored approach to genetic testing for specific conditions. Through case examples, we highlight the power and impact of our clinic. By integrating ophthalmic care with medical genetics and counseling, the MOGC has not only helped solve individual patient diagnostic challenges but has aided the greater population in novel genetic discoveries and research towards targeted therapeutics.

摘要

密歇根大学凯洛格眼科中心的多学科眼科遗传学诊所 (MOGC) 旨在为患有遗传性眼部疾病的患者提供医疗和眼科遗传学护理。我们制定了临床和转诊工作流程,每位患者都由我们的多学科团队进行协调评估,然后就诊断、预后和基因检测进行讨论。检测方法针对每个患者具体情况而定,可以是靶向的(单基因、基因panel),也可以是广泛的(染色体微阵列、全外显子组测序),或者两者结合。我们假设这种诊所模式可以改善患者的治疗效果和护理质量。对 2020 年 7 月至 2022 年 10 月期间 MOGC 患者的回顾性图表审查显示,最常见的转诊诊断是先天性白内障、视神经病变和小眼球,其中 52%为综合征病例。在这一患者群体中,我们看到 76%的患者接受了基因检测,其中 33%获得了诊断性检测结果。我们的结果支持针对特定疾病进行定制化的基因检测方法。通过案例示例,我们强调了我们诊所的强大功能和影响力。通过将眼科护理与医学遗传学和咨询相结合,MOGC 不仅帮助解决了个别患者的诊断难题,还为更大的人群在新的遗传发现和针对特定治疗的研究方面提供了帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/10048684/873992421327/genes-14-00726-g001.jpg

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