Myotonic dystrophy is a multi-system disorder affecting skeletal muscle, brain, heart, and other organs commonly found in adults and is caused by either CTG (DM1; Myotonic dystrophy type 1) or CCTG (DM2; Myotonic dystrophy type 2) pathogenic repeat expansions of either DMPK (DM1) or ZNF9 (DM2) RNA transcripts [74, 75]. The gene discussed is CNBP; the disease is myotonic dystrophy type 1.