Genetic Test Details
Muscular Dystrophies Panel
Test Information
- Titre
-
Muscular Dystrophies Panel
- Catégorie
- Neurogenetics
- Sub Category
-
Neuromuscular Disease
- Gene/Platform/Region List
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ACADVL, ANO5, ATP2A1, BAG3, BVES, CAPN3, CAV3, CAVIN1, COL6A1, COL6A2, COL6A3, CPT2, CRPPA, CRYAB, DAG1, DES, DMD, DNAJB6, DNMT3B, DOK7, DPM3, DYSF, EMD, FHL1, FKRP, FKTN, FLNC, GAA, GGPS1, GMPPB, GNE, GOSR2, HNRNPDL, JAG2, KBTBD13, LAMA2, LAMP2, LARGE1, LIMS2, LMNA, LPIN1, LRIF1, MTM1, MYH7, MYOT, ORAI1, PFKM, PHKA1, PLEC, POGLUT1, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POPDC3, PYGM, PYROXD1, RYR1, SELENON, SGCA, SGCB, SGCD, SGCG, SMCHD1, STIM1, SYNE1, SYNE2, TAFAZZIN, TCAP, TK2, TMEM43, TNPO3, TOR1AIP1, TRAPPC11, TRIM32, TTN, VCP, VMA21
- Test type
- Gene Panel
- Samples Accepted
- Blood, DNA
- Indications
- Carrier Cascade Testing, Diagnostics
- Test Methodology
- Sequencing
- Disease/Condition
-
Muscular Dystrophies, Congenital Muscular Dystrophy (CMD), Limb-girdle Muscular Dystrophy (LGMD), Emery-Dreifuss muscular dystrophy (also called scapulo-peroneal), dystrophinopathy (Duchene Muscular Dystrophy and Becker Muscular Dystrophy), Oculopharyngodistal myopathy, Facioscapulohumeral muscular dystrophy (FSHD), and myotonic dystrophy
Dernière Mise à Jour: 06 janvier 2026
