Diagnosis

Your doctor will do a physical examination ― including a neurological exam ― and review symptoms and medical history to check for signs of a congenital myasthenic syndrome. Your doctor may also order tests to exclude other conditions with similar symptoms.

The following tests can help diagnose a congenital myasthenic syndrome and determine how severe the disorder is.

  • Blood tests. A blood test might reveal the presence of abnormal antibodies that disrupt signals between your nerves and your muscles. Other blood tests may be helpful to rule out other conditions that may have similar symptoms.
  • Electromyography (EMG). EMG is a diagnostic procedure to assess the health of muscles and the nerve cells that control them, called motor neurons. EMG results can reveal nerve dysfunction, muscle dysfunction or problems with signal transmission between the nerves and muscles.
  • Repetitive nerve stimulation. In this nerve conduction study, electrodes are attached to your skin over the muscles to be tested. Small pulses of electricity are sent through the electrodes to measure the nerve's ability to send a signal to your muscle. The nerve is tested repeatedly to see if its ability to send signals worsens with fatigue.
  • Genetic testing. This can identify the specific affected gene that's responsible for the congenital myasthenic syndrome and which treatments may be beneficial.
  • Cholinesterase challenge test. Cholinesterase inhibitor medication, such as pyridostigmine, is given to determine if improvement in muscle fatigue occurs with repetitive movement.
  • Other tests. These may include lung function tests to assess breathing and oxygenation, a sleep study to assess breathing and apnea during sleep, or a muscle biopsy to look at muscle fibers.

Genetic testing

Genetic testing involves examining your DNA, the chemical database that carries instructions for your body's functions. Genetic testing can reveal changes, sometimes called mutations, in genes that cause congenital myasthenic syndromes. Genetic testing may also be recommended for family members.

Talking to your doctor, a medical geneticist or a genetic counselor about why the test is being done and how the results may affect you is an important step in the process of genetic testing.

Treatment

Rarely, some children with mild congenital myasthenic syndromes may not need treatment.

Medication

Medications aren't a cure, but they can improve muscle contraction and muscle strength in people with congenital myasthenic syndromes. Which medications are effective depends on the type of affected gene. Medications that are effective for one type of syndrome may be ineffective for another type, so genetic testing is recommended before starting medications.

Medication treatment options may include:

  • Acetazolamide
  • 3,4-diaminopyridine (3,4-DAP), marketed as amifampridine (Firdapse, Ruzurgi)
  • Albuterol
  • Ephedrine
  • Fluoxetine (Prozac)
  • Neostigmine (Bloxiverz)
  • Pyridostigmine (Mestinon, Regonol)

Supportive treatments

Supportive treatments depend on the type and severity of the congenital myasthenic syndrome. Options may include:

  • Therapies. Physical, speech and occupation therapies may help maintain function. Therapy also can offer supportive devices, such as wheelchairs, walkers, and hand and arm supports.
  • Breathing support. Some congenital myasthenic syndromes may result in pauses in breathing, called apnea. Using an apnea monitor may be recommended. Noninvasive positive-pressure ventilation, such as a continuous positive airway pressure (CPAP) mask and machine, may be used to support breathing and oxygenation. In some cases, intubation and use of mechanical ventilation may be needed.
  • Feeding support. Problems with chewing and swallowing may require additional nutrition. Enteral nutrition, also known as tube feeding, is a way of delivering nutrition directly into the stomach or small intestine. Your doctor may recommend a procedure to place a tube through the skin on the abdomen and into the stomach (gastrostomy) or into the small intestine (jejunostomy).
  • Surgery. For severe orthopedic deformities, such as in the spine or feet, surgical correction may be needed.

Ongoing care

Regular follow-up appointments with a team of medical professionals provides ongoing care and may help prevent certain complications. Your health care team can link you with appropriate support for home, school or work.

Pregnancy can worsen symptoms of congenital myasthenic syndromes, so close monitoring during and after pregnancy is required.

Coping and support

Caring for a child or family member with a congenital myasthenic syndrome can be stressful and exhausting. You may not know what to expect, and you may worry about your ability to provide the care needed.

Consider these steps to prepare yourself:

  • Learn about the disorder. Learn as much as you can about congenital myasthenic syndromes. Then you can make the best choices and be an advocate for yourself or your child.
  • Find a team of trusted professionals. You'll need to make important decisions about care. Medical centers with specialty teams can offer you information about the disorder, coordinate your care among specialists, help you evaluate options and provide treatment.
  • Seek out other families. Talking to people who are dealing with similar challenges can provide you with information and emotional support. Ask your doctor about support groups in your community. If a group isn't for you, maybe your doctor can put you in touch with a family who has dealt with the disorder. Or you may be able to find a group or individual support online.
  • Consider support for caregivers. Ask for or accept help in caring for your loved one when needed. Options for additional support can include asking about sources of respite care, asking for support from family and friends, and taking time for your own interests and activities. Counseling with a mental health professional may help with adjustment and coping.

Preparing for your appointment

Make an appointment with your doctor if you notice signs or symptoms common to congenital myasthenic syndromes. After the initial evaluation, you may be referred to a doctor trained in evaluating and treating these conditions.

Here's some information to help you prepare for your appointment, as well as what to expect from your doctor.

What you can do

You may want to prepare answers to these questions:

  • What symptoms do you notice?
  • When did the symptoms start?
  • Does anything make the symptoms better or worse?
  • Has anyone in your family ever had a congenital myasthenic syndrome?

What to expect from your doctor

After getting detailed information about the symptoms and your family's medical history, your doctor may order tests to help with diagnosis and plan treatment.

By Mayo Clinic Staff