🧬 Myotonic Dystrophy DMPK Gene Analysis at MedEx Neo Clinic, Kathmandu 📍 The Myotonic Dystrophy DMPK gene analysis at MedEx Neo Clinic Kathmandu detects CTG trinucleotide repeat expansions in the DMPK gene, which are the genetic cause of Myotonic Dystrophy type 1 (DM1). This inherited neuromuscular disorder results in progressive muscle wasting and weakness, myotonia, cardiac conduction defects, and endocrine abnormalities. The test uses advanced PCR and Southern blot techniques to determine the size of repeat expansions for diagnosis, prognosis, and genetic counseling. MedEx Neo Clinic provides precise molecular genetic testing with confidential results and expert interpretation.