Genetic testing for Kennedy's disease (spinal and bulbar muscular atrophy) in the AR gene

An increase in the number of CTG triplet repeats (expansion) in the 3'-untranslated region of the DMPK gene is the cause of myotonic dystrophy type 1, a common autosomal dominant neurological disorder.

Within 12 days. The specified time does not include the day of biomaterial collection