Rare diseases: Duchenne muscular dystrophy

Medicover Genetics Editorial Team|

Scientifically checkedView our editorial guidelines
Scientifically checked

Duchenne muscular dystrophy is a rare inherited muscle disorder characterized by progressive muscle weakness and degeneration that leads to difficulties walking and reduces life expectancy. It is a single gene disorder that is caused by genetic changes in the DMD gene. Our latest infographic is all about Duchenne muscular dystrophy, and it includes facts about the DMD gene and information on the disease symptoms and current treatment, as well as summarizing promising research into future treatments.

You can learn more about Duchenne muscular dystrophy and genetic testing for this and other muscular disorders .

Topics covered in this infographic:

  • What causes Duchenne muscular dystrophy?
  • The DMD gene
  • Dystrophin
  • Why does it affect mostly men?
  • Symptoms
  • Genetic testing
  • Disease management and treatment
  • Research and development

Last updated: 14.09.2026

Latest articles

All about genetics
Health and well-being
Hereditary diseases

  • VERACITY

    New-generation non-invasive prenatal screening from week 9 of pregnancy, analysing fetal cell-free DNA in maternal blood to detect selected chromosomal abnormalities with high sensitivity and specificity for early and reliable prenatal risk assessment.

  • Pharmacogenomics

    Enabling personalised treatments for safer, more effective care through genetic insights that guide optimal prescribing from the start and refine therapy when patients experience side effects or poor response.

  • ebiom+

    A comprehensive assessment of the endometrial microbiome and chronic endometritis pathogens to enhance clinical outcomes, prevent treatment delays, and support a more informed, personalised fertility care.

  • WES

    Advanced sequencing that simultaneously analyses a broad range of genes to detect the genetic basis of complex diseases, improve diagnostic accuracy, and inform recurrence risk assessment for better clinical decision-making.

Why Medicover Genetics

Leader in genetic testing with >25 years of experience in counselling and diagnostics

Comprehensive CE-IVD kit portfolio and seamless Technology Transfer solution for laboratories of any size

End-to-end clinical workflow from sample processing to sequencing analysis and reporting

CAP- and CLIA- and ISO15189 accredited, GMP- and ISO9001 and 13485 certified

Are you a patient?

Are you a physician?