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KMID : 1100820230130030141
Laboratory Medicine Online
2023 Volume.13 No. 3 p.141 ~ p.153
Practical Guidelines for Chromosomal Microarray Analysis for Constitutional Abnormalities: Part I, General and Prenatal
Seol Chang-Ahn

Ha Jung-Sook
Won Dong-Joo
Kim In-Suk
Abstract
Chromosomal microarray (CMA) testing can enhance the quality of clinical care for congenital abnormalities, including prenatal diagnosis. Laboratories require a comprehensive understanding of the strengths, weaknesses, and purposes of CMA testing. They should also have appropriate plans, guidelines, and documented records for platform validation and quality control at all stages of testing. Performing prenatal CMA testing necessitates understanding the features of prenatal specimens, devising a verification process, reporting results, and providing genetic counseling. This guideline aims to establish standard test protocols for conducting CMA tests, ensuring accurate results, and aiding in diagnosing and treating patients.
KEYWORD
Congenital abnormalities, DNA copy number variations, Microarray analysis, Prenatal diagnosis
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