The 20 Best Myofibrillar Myopathy Doctors Near Me in burien, WA

Find the Top Myofibrillar Myopathy Experts and Specialists

Last Updated: 09/26/2026

Save doctors for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Already have a doctor?
Find A Second Opinion

MediFind found 1 doctor with experience in Myofibrillar Myopathy near burien, WA. Of these, 1 are Experienced.

Location
LocationClose
1 provider found
    Experienced in Myofibrillar Myopathy
    Experienced in Myofibrillar Myopathy
    Referral may be required

    Franciscan Neurology Associates At St. Anne

    16259 Sylvester Road SW, Suite 503, 
    Burien, WA 
     (1.2 miles away)
    206-835-7440
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients
    Offers Telehealth

    Emmanuel Martinez is a Neurologist practicing medicine in Burien, Washington. Dr. Martinez is rated as an Experienced provider by MediFind in the treatment of Myofibrillar Myopathy. He is also highly rated in 18 other conditions, according to our data. His clinical expertise encompasses Partial Familial Epilepsy, Tension Headache, Seizures, and Partial Seizure. Dr. Martinez is board certified in Neurology, American Board Of Psychiatry And Neurology, Clinical Neurophysiology, American Board Of Psychiatry And Neurology, and Epilepsy, American Board Of Psychiatry And Neurology. Dr. Martinez is currently accepting new patients.

    Learn about our expert tiers
    Showing 1-1 of 1

    Last Updated: 09/26/2026

    What is the definition of Myofibrillar Myopathy?

    Myofibrilar myopathy (MFM) is a neuromuscular disease characterized by slowly progressive muscle weakness that can involve both proximal muscles (such as hips and shoulders) and distal muscles (those further away from the trunk). Some affected individuals also experience muscle stiffness, aching, or cramps. Other symptoms that can be associated with MFM include pain and tingling in the limbs (peripheral neuropathy) or an enlarged and weakened heart (cardiomyopathy). Most people with MFM begin to develop muscle weakness in mid-adulthood, but features of the disease can appear anytime between infancy and late adulthood. MFM is caused by a genetic change (change) in any of several genes, including DES, CRYAB, MYOT, LDB3, FLNC, BAG3, FHL1, TTN, and DNAJB6. The signs and symptoms of MFM can vary depending on the genetic cause. For some people, the exact genetic cause may be unknown. The mode of inheritance of the disease depends on exactly which gene is changed. MFM can be diagnosed with a muscle biopsy or other studies of muscle function. The diagnosis can be confirmed with genetic testing.