How is muscular dystrophy diagnosed

In this section, we’ll explore key components of the diagnostic journey: Firstly, physical assessments, with a particular focus on neuromuscular assessments. Secondly, looking at the various testing methods including blood tests (specifically creatine kinase levels), genetic testing and muscle biopsies, where we will even delve into histology images, helping you understand what’s happening in the muscles.

Additionally, we’ll discuss the circumstances in which muscle biopsies are performed, giving you insight into when and why this procedure might be necessary in the diagnostic process. Together, we’ll navigate the path towards a better understanding of Duchenne muscular dystrophy.