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    MYOTONIC DYSTROPHY ZFN9 GENE ANALYSIS

    Detects CTG repeat expansions in ZNF9 gene causing Myotonic Dystrophy type 2.

    Chhusya Bahal (Chhusya Galli), Jyatha, Thamel, Kathmandu 44600, Bagmati
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    Description
    🧬 Myotonic Dystrophy ZFN9 Gene Analysis at MedEx Neo Clinic, Kathmandu 📍 The Myotonic Dystrophy ZFN9 gene analysis offered by MedEx Neo Clinic Kathmandu focuses on detecting abnormal CTG repeat expansions in the ZNF9 (also called CNBP) gene associated with Myotonic Dystrophy type 2 (DM2). DM2 is a multisystemic muscular disorder characterized by muscle pain, stiffness, cataracts, and cardiac issues. Molecular testing through repeat-primed PCR allows precise diagnosis, helping differentiate DM2 from other myopathies and facilitating patient management and family counseling. MedEx Neo Clinic delivers reliable genetic diagnostics with expert clinical support.
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    MYOTONIC DYSTROPHY ZFN9 GENE ANALYSIS

    17,250 NPR