Búsqueda

Diagnosis 4

Dealing With the Diagnosis _ If your child or young person DOES have DMD: Resources and therapies are available to help manage symptoms and possibly slow down the progression of the condition. If your child or young person DOES NOT have DMD: Your doctor will do more investigations into what else could be causing symptoms. […]

Diagnosis 3

What Will the Doctor Do to Diagnose DMD? _ How DMD is diagnosed Confirming signs and symptoms If Duchenne muscular dystrophy (DMD) is suspected, the first thing your family doctor will do is perform a physical exam to check for muscle weakness. They will also ask about delays in early developmental milestones, such as sitting, […]

Diagnosis 2

When is the Right Time to Talk to a Doctor? _ Helping your doctor reach a diagnosis Take these three steps to prepare for the doctor’s visit and help them determine whether it is DMD or another condition; Helping your doctor reach a diagnosis Understanding your family’s history of muscle disease and other conditions can […]

Diagnosis 1

How Do You Know It’s Duchenne Muscular Dystrophy (DMD)? _ Only a doctor can make a DMD diagnosis. There are a specific set of steps the doctor will go through that will help them tell whether a patient has DMD. Doctors will look at: Signs and symptoms of DMD Results of a blood test for […]

en_USEnglish

You are about to view a website that PTC Therapeutics has not reviewed for accuracy, relevance or completeness.

PTC Therapeutics does not endorse organizations that sponsor linked external websites, products, or services that such organizations may offer; and does not control or guarantee the currency, accuracy, relevance or completeness of the information found on the linked external sites.

All trademarks includes herein are the property of their respective owners.

Why Sign Up?

Sign up to receive the latest information from the Duchenne muscular dystrophy community. Be the first to receive:

News alerts

Content updates

Latest resources

Ongoing support

Name

Email

Country

Address

Have you been diagnosed with DMD?

What type of DMD mutation do you have?

This site is intended for US residents only.
The information on this site is not intended to make a diagnosis or to take the place of talking to a US health care professional.

PTC Cares™ is a trademark of PTC Therapeutics.
© 2022 PTC Therapeutics, Inc. All rights reserved.

Date of preparation: September 2022
MAT-CORP-0268

Important Terms and Concepts

Basic terms and key definitions

Neuromuscular disorders

Neuromuscular disorders affect the muscles and nerves, and most of the causes are genetic. This means they are either passed down through the family or caused by changes in an individual person’s genes.

Most neuromuscular disorders cause muscle weakness that worsens over time. Signs and symptoms of neuromuscular diseases can vary and may be mild, moderate, or severe.

Most often, when a child has a neuromuscular disease, they don’t grow and develop as fast as other children their age. They are often slow to start lifting their head, sitting, walking, and talking.

Treatment and supportive care may improve the symptoms of a neuromuscular disorder, increasing mobility and even life expectancy.

Muscular dystrophy

Muscular dystrophy is the term for a group of neuromuscular disorders that cause muscle weakness and muscle loss.

Duchenne muscular dystrophy (DMD) is a type of muscular dystrophy that causes muscle weakness that worsens over time. The progression and symptoms can vary from person to person.