Duchenne Muscular Dystrophy (DMD) Program

Duchenne Muscular Dystrophy (DMD) Program

Duchenne Muscular Dystrophy (DMD) Program

The Duchenne Muscular Dystrophy (DMD) Program at Children's Health℠ is one of the most comprehensive in Texas.

Our clinic is a certified Duchenne Care Center by the Muscular Dystrophy Association and the Parent Project Muscular Dystrophy. We treat children of all ages, from diagnosis to their transition to adult care.

Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy and typically affects boys. It usually starts between ages 2 and 5 and affects many aspects of a child’s health, from their ability to walk to the strength of their heart and breathing muscles.

Children’s Health neuromuscular disease experts understand the specific ways that muscular dystrophy affects breathing, heart function and other aspects of health. We collaborate with specialists from pulmonology, cardiology, rehabilitation medicine, orthopedics, endocrinology and nutrition to give patients the best possible care.

We use preventive care to keep your child’s body strong and avoid complications. Our preventive approach includes devices that help support breathing to prevent respiratory illness, and heart medication that helps kids stay healthy and active.

We also prioritize normalizing everyday tasks and experiences like getting ready for school, playing with friends and getting around the community. Together, we are ready to help your child retain their strength, prepare for changes.

Dallas

214-456-2768
Fax: 214-456-6898
Ste F5400

 

New patient referral fax:
214-456-6255

 

For new patient referrals, please include patient demographic sheet, pertinent labs, imaging reports, office notes, and insurance information.

 

Request an Appointment with codes: Neurology

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Accepted Insurance Plans

Conditions We Treat

  • Central Core Disease
  • Congenital Muscular Dystrophy (MD)
  • Congenital Myasthenic Gravis Syndrome
  • Duchenne Muscular Dystrophy (DMD)/Becker Muscular Dystrophy (BMD)
  • Emery-Dreifuss Muscular Dystrophies
  • Facioscapulohumeral Muscular Dystrophy (FSH)
  • Friedreich’s Ataxia
  • Limb-Girdle Muscular Dystrophy (LGMD)
  • McArdle Disease
  • Metabolic Neuropathies
  • Mitochondrial Disorders
  • Myotonia Congenita
  • Nemaline Myopathy
  • Periodic Paralysis
  • Pompe Disease

Our Programs

Treatments and Services

There is no cure for muscular dystrophy. However, some medications are able to slow muscle weakening and many physical therapies help strengthen muscles lungs, preserve mobility and independence. Our DMD team works together to design a personalized care plan for each patient that is based on:

  • The child's age
  • Overall health and medical history
  • The progression of the duchenne muscular dystrophy
  • The child’s ability to tolerate different medications, procedures and therapies
  • Expectations for the course of the condition
  • Family needs and priorities

Non-surgical care to help manage symptoms

  • Physical and occupational therapy to build strength, maintain flexibility and support everyday movements
  • Speech therapy improve communication when face muscles weaken
  • Respiratory therapy to help with breathing
  • Regular cardiac evaluations
  • Positioning aids used to help the child sit, lie or stand
  • Braces, splints and wheelchairs to prevent deformity, promote support and provide protection
  • Medication
  • Nutritional counseling and diet planning

Surgical care to manage complex symptoms

  • Procedures to correct scoliosis (a sideways curvature of the back bones) and joint contractures
  • Surgery to implant a pacemaker for heart problems
  • Surgery to remove cataracts

Learn more about treatment with Elevidys

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Duchenne Muscular Dystrophy (DMD)

Together, we can change the future of patients with Duchenne Muscular Dystrophy (DMD).

A World-Class pediatric Duchenne Muscular Dystrophy program

When you first come to the Duchenne Muscular Dystrophy (DMD) program, your child will receive a whole-body assessment that will include physical tests, blood tests and muscle biopsies.

Children’s Health experts understand the specific ways that muscular dystrophy affects breathing, heart function and other aspects of your child’s health.

The most common programs and clinics our patients receive care from include:

We also actively pursue new and better ways to treat DMD through research and clinical trials. Ongoing research includes studies for advanced techniques like gene therapy and exon-skipping technology, which aims to restore a protein that doesn’t work properly in patients with DMD.

Convenient, coordinated muscular dystrophy care

Usually, muscular dystrophy care requires patients to juggle several appointments at different medical offices. This can require traveling great distances and missing multiple days of school.

At our clinic, we schedule appointments so that your child sees all their doctors in a single visit. This multidisciplinary appointment is more convenient for you and your child. It also enables our team to work together and quickly move forward with the care your child needs.

Living with Pediatric Duchenne Muscular Dystrophy

Children with duchenne muscular dystrophy will experience muscle weakness throughout life. Eventually their muscles will start to break down causing them to need progressively more acute care and support.

DMD patients develop enlarged calf muscles, while their thigh muscles become thin. Their tongue and forearm muscles may also become enlarged. Progressive joint stiffening will reduce their flexibility and limit their ability to move independently.

Many children will develop severe spinal curvature (scoliosis).

Pulmonary complications are also common due to weakness in chest and throat muscles. When this happens, children have difficulty coughing and swallowing, which can cause frequent lung infections. Eventually, the heart muscles will begin to break down, causing cardiomyopathy.

Support for the child and family

We take extra steps to help kids live well with DMD, and we support families throughout the care journey. We take time to educate families on the disease and how this condition can affect their lives. We’re there to help with every aspect of living with DMD, from working with schools to getting wheelchairs and making other accessibility changes.

We also aim to have each child to see themselves as capable as every other child. Our team will integrate your child’s wants and needs into their treatment and use those goals as motivation to pursue new milestones. We have a number of resources to participate in adaptive sports and other activities.

Coordinated care for complex needs

Some children may eventually need surgery for scoliosis, cataracts or heart problems. Your child’s DMD team will work closely with the inpatient care team to plan their recovery and new therapeutic needs.

All DMD patients will eventually need extensive heart and lung care. A cough-assist machine will help your child get a deeper breath and clear their airway. Many Duchenne patients eventually need a machine to help with breathing (bilevel positive airway pressure, Bi-PAP). Medicines can help the heart move blood around the body and some will need a pacemaker.

Partnering with other clinics

Some families find regular outpatient care close to their home or school. We can partner with specialists in your area and can continue to provide specialty care as needed.

Children's Health Resources

Meet the Care Team

At Children’s Health, our muscular dystrophy team includes experts in neurology, cardiology, pulmonology, gastroenterology and physical therapy. Our specialists work together and create a care plan that’s customized to your child’s specific needs.

Locations

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