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Lahalak Medical PlatformDifferentiate Care
CHD7 Gene Deletion and Duplication Analysis (CHARGE Syndrome)
This advanced genetic test accurately diagnoses CHARGE syndrome by detecting structural changes in the CHD7 gene, enabling early intervention and personalized medical care for patients with multiple congenital anomalies.
A specialized laboratory test to detect deletions or duplications in the CHD7 gene. It evaluates patients with multiple congenital anomalies to confirm the diagnosis of CHARGE syndrome.
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