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Lahalak Medical PlatformDifferentiate Care
KMT2D Gene Deletion/Duplication Analysis
Identify the genetic causes of Kabuki syndrome with high precision by analyzing copy number variants in the KMT2D gene, enabling early diagnosis and comprehensive care planning.
An advanced genetic test detecting deletions or duplications in the KMT2D gene associated with Kabuki syndrome type 1. It identifies copy number variants often missed by standard sequencing.
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