Oculopharyngeal Muscular Dystrophy (OPMD)
What is oculopharyngeal muscular dystrophy?
Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic condition. It causes weakness in the muscles around the upper eyelids and part of the throat called the pharynx. The condition may affect vision and cause problems swallowing and talking.
OPMD affects both men and women. It often first appears between 40 and 60 years of age. As the disease slowly gets worse, the muscle weakness can extend into the neck and shoulders. In time, OPMD may affect the arms and legs and lead to trouble with walking. OPMD generally does not shorten a person’s life span.
What causes oculopharyngeal muscular dystrophy?
OPMD is caused by a genetic problem. The problem is in a gene that has the information needed to make a protein called polyadenylate-binding protein (PABPN1). The defect leads to a buildup of PABPN1 in the muscle cells. The PABPN1 clumps inside the muscle cells and may cause the cells to die. This leads to muscle weakness.
The defective gene that causes OPMD is passed down from a parent to his or her child. Most often, a person with the disease has only one copy of the gene defect. In some cases, a person might get two copies of the gene, one from each parent. This may lead to more severe OPMD. The disease will get worse more quickly. OPMD is more common in:
OPMD also happens in people who are not part of these groups.
What are the symptoms of oculopharyngeal muscular dystrophy?
OPMD usually first affects people in their 40s and 50s. The condition generally affects the muscles in the upper eyelids and throat. You may first notice drooping eyelids or trouble swallowing. Most of the time, OPMD gets worse very slowly. Common symptoms include:
Eyelid drooping. This may be severe enough to need special glasses to brace the eyelids open or surgery to raise the eyelids.
Choking or swallowing problems (dysphagia). Dry foods may be the first to cause trouble. But swallowing liquids can later be a challenge.
Pooling of saliva
Facial muscle weakness
Leg and arm weakness
About 1 in 25 to 1 in 10 people with OPMD may develop more severe upper leg weakness. They may need to use a wheelchair.
How is oculopharyngeal muscular dystrophy diagnosed?
The doctor will take your health history, and ask about your recent symptoms, past health conditions, and family health history. The doctor will do a thorough physical exam, including checking the muscles around your eyes. The provider may test how well you can swallow. Your test may include:
DNA tests (blood tests) to look for gene defects
Timed swallowing tests
Video studies of swallowing
Nerve conduction studies and electromyography (EMG)
Muscle biopsy to look for OPMD PABPN1 clumps. This is often not needed if the genetic tests are clear.
Blood tests to help rule out other conditions
You may first see your main doctor and then get a referral to a neurologist. Some neurologists specialize in neuromuscular diseases such as OPMD.
How is oculopharyngeal muscular dystrophy treated?
Treatment for OPMD focuses on helping the swallowing problems, eyelid drooping, or limb weakness.
Because the tongue and throat muscles are weak in OPMD, moving food from your mouth into your esophagus becomes tricky. This can cause choking and breathing food into your lungs. This may lead to pneumonia. Changing the texture of your foods may make them easier to swallow. In some cases, procedures to help make swallowing safer and more comfortable may help.
One such procedure widens the opening in a muscle just above the top of your esophagus. The aim is to make it easier for food to move past this muscle into your esophagus. A doctor can widen the muscle with a dilating tool. Or they can widen it by injecting botulinum toxin into the muscle to help relax it. This procedure only helps in the short term. You may need to have it repeated. A surgical cut into the muscle can be a more permanent solution for swallowing problems. In some cases, you may need to bypass the throat completely and use a feeding tube instead.
Surgery may also help correct severe eyelid drooping. Drooping eyelids can interfere with vision, driving, and other activities. Eyelid surgery (blepharoplasty) or tightening the muscle that lifts the eyelid may help. In some cases, a sling can attach the eyelid to the forehead muscle to help keep the lid open.
The benefits from both of these treatments may last for only several years.
Occupational therapy can help you find ways to adapt to arm and leg weakness. You may benefit from leg braces, canes, or walkers.
What are possible complications of oculopharyngeal muscular dystrophy?
In severe OPMD, upper leg weakness may require you to use a wheelchair. This is rare, though.
The main complications of OPMD have to do with swallowing problems (dysphagia). This can lead to weight loss and nutrition problems. It can also cause choking and the breathing of food, saliva, liquids, or stomach contents into the lungs (aspiration). This can lead to infections and cause pneumonia, which can be fatal. You may need a procedure to reduce the risk for aspiration. Most people with OPMD have normal lifespans.
How to manage oculopharyngeal muscular dystrophy
OPMPD usually develops after age 40 and gets worse slowly. A speech-language pathologist SLP can teach you ways to deal with speech or swallowing problems related to OPMD. These may include swallowing techniques and strategies for talking. An occupational therapist can help you with adaptive methods for daily tasks. You may also find a cane, walker, or other walking aid helpful if the OPMD affects your leg muscles.
It’s important to work with your healthcare team to address any swallowing issues. Strategies such as changing the texture of food, taking smaller bites, or holding your head in certain ways while swallowing may be helpful. You may need to have a procedure to make swallowing safer and more comfortable. You may need to see a nutritionist to make sure you get enough nutrition if you use a feeding tube.
You and your family may find support from organizations such as the Muscular Dystrophy Association.
Key points about oculopharyngeal muscular dystrophy
OPMD is a rare genetic condition that causes weakness in the muscles around the upper eyelid and throat.
OPMD affects both men and women, usually first appearing in people after 40 years of age.
The first symptoms are eyelid drooping and trouble swallowing.
The swallowing problems increase the risk for potentially fatal aspiration pneumonia.
You may need procedures to help with swallowing or other problems.
Tips to help you get the most from a visit to your healthcare provider:
Know the reason for your visit and what you want to happen.
Before your visit, write down questions you want answered.
Bring someone with you to help you ask questions and remember what your provider tells you.
At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you.
Know why a new medicine or treatment is prescribed, and how it will help you. Also know what the side effects are.
Ask if your condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if you do not take the medicine or have the test or procedure.
If you have a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your provider if you have questions.
Online Medical Reviewer:
Anne Fetterman RN BSN
Online Medical Reviewer:
Joseph Campellone MD
Online Medical Reviewer:
Raymond Kent Turley BSN MSN RN
Date Last Reviewed:
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