Chromosomal Microarray in Prenatal Diagnosis: A Single Center Experience From Türkiye

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Observational analysis recorded 4.8% pathogenic variants in prenatal samples from Türkiye, indicating CMA's importance for genetic counseling.

CMA successfully identified 21 pathogenic variants in 373 prenatal samples, emphasizing its diagnostic value.
About 4.8% of cases showed significant genetic alterations, showcasing CMA's relevance in detecting fetal anomalies.
The study involved evaluating ultrasound findings and family history for effective use of CMA in prenatal diagnosis.
CMA results stress the necessity for reporting unique breakpoints, which aids in genetic counseling and management.

Kayhan et al. (2025) studied this question.

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Observational analysis recorded 4.8% pathogenic variants in prenatal samples from Türkiye, indicating CMA's importance for genetic counseling.