The landscape of Duchenne is rapidly changing!
New therapies are being developed, some of which will help any person with Duchenne, while others depend on the person's genetic change, or mutation. Knowing the mutation is important, as it can affect decision-making about the possible use of new therapies and entering into clinical trials.
Duchenne is caused by changes (mutations) within the dystrophin gene. A gene is made up of coding regions call "exons," and the areas in between exons called "introns." Dystrophin has 79 exons, which makes it the largest gene in the body.
Genetic testing can identify your/your child's specific mutation. If you/your child need genetic testing, please talk with your doctor, genetic counselor, or one of the The Duchenne Registry genetic counselors.
Making the dystrophin protein from the gene involves several steps. One of the first steps is removing the introns and fitting the exons together, 1-79, like puzzle pieces.

exon map of the dystrophin gene
If there is a missing piece within the dystrophin gene (deletion) or an extra piece (duplication), your body can have difficulty making dystrophin. The most common genetic mutation causing Duchenne is a deletion, where part of the gene is missing.
One approach that strives to address this lack of dystrophin is exon skipping, which tells the body to hide an exon next to the missing piece, so the whole section can be skipped over and the remaining exons can fit together. The intent is to allow the body to make a shorter form of the dystrophin protein. The tool below will help you to know whether your/your child's genetic mutation might benefit from an exon skipping therapy.

missing exon

skipped exon