现型驱动的分子遗传测试建议用于诊断儿科罕见疾病
Fangyi Chen1, Priyanka Ahimaz2,3, Kai Wang4
1Department of Biomedical Informatics, Columbia University, New York, NY, USA.
Research square
|December 4, 2023
概括
诊断罕见疾病是具有挑战性的. 基于表型的分子遗传测试建议 (Phen2Test) 可以帮助临床医生选择适当的遗传测试,提高罕见儿科疾病的诊断效率.
科学领域:
- 基因组医学是基因组医学.
- 罕见疾病的诊断 罕见疾病的诊断
- 临床决策支持 临床决策支持
背景情况:
- 罕见病患者面临长期的诊断延迟,通常是由于选择适当的遗传测试的挑战.
- 在遗传测试选择工作流程中,表型信息未得到充分利用,阻碍了及时诊断.
结论:
- 现型特征对于指导罕见疾病诊断中的遗传测试选择非常有价值.
- Phen2Test提供了一个实用的解决方案,以减少诊断的奥德赛和提高基因测试的效率.
- 这种方法支持将基因组医学纳入常规临床实践,提高诊断能力.
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