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Lahalak Medical PlatformDifferentiate Care
CYP21A2 Gene Deletion/Duplication Analysis
A precise genetic test to detect mutations in the CYP21A2 gene, aiding in the early diagnosis of congenital adrenal hyperplasia and ensuring appropriate medical care from the start.
A specialized laboratory test to detect deletions or duplications in the CYP21A2 gene, which causes 21-hydroxylase deficiency in congenital adrenal hyperplasia, supporting accurate genetic diagnosis.
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