Noninvasive prenatal testing in China: Future detection of rare genetic diseases?

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Abstract

conditions in fetuses using a maternal blood sample, thus avoiding the risk of miscarriage associated with traditional invasive procedures. Since 80% of rare diseases are genetic diseases, NIPT has the potential to detect rare genetic diseases early on and it has been used in many countries and regions. Since China has the world's largest population of patients with rare diseases, NIPT has been implemented in China since 2010. However, the regulations governing NIPT in China are weak and NIPT oversight and research are still lacking. Strict registration is needed to ensure the quality of NIPT, additional certification can help a developer/manufacturer of an NIPT test to compile clinical data and to improve innovation, and academic societies can provide committee opinions that are suited to the current situation in China. These efforts may improve regulations governing NIPT and NIPT oversight and research in China. With these improvements, NIPT may offer promise in terms of the early detection of rare diseases. © 2014, International Research and Cooperation Association for Bio & Socio-Sciences Advancement. All rights reserved.

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APA

Lin, M., Qi, T., Baiyu, S., & Lingzhong, X. (2014). Noninvasive prenatal testing in China: Future detection of rare genetic diseases? Intractable and Rare Diseases Research, 3(3), 87–90. https://doi.org/10.5582/irdr.2014.01012

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