The 20 Best Myofibrillar Myopathy Doctors Near Me in Penza, RU

Find the Top Myofibrillar Myopathy Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 5 doctor with experience in Myofibrillar Myopathy near Penza, RU. Of these, 3 are Experienced and 2 are Advanced.

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5 providers found
    Advanced in Myofibrillar Myopathy
    Advanced in Myofibrillar Myopathy
    49 Kronverkskiy Ave, 
    Saint Petersburg, SPE, RU 

    Anna Kostareva practices practicing medicine in Saint Petersburg, Russian Federation. Ms. Kostareva is rated as an Advanced expert by MediFind in the treatment of Myofibrillar Myopathy. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Restrictive Cardiomyopathy (RCM), Familial Progressive Cardiac Conduction Defect, Emery-Dreifuss Muscular Dystrophy, Heart Bypass Surgery, and Heart Transplant.

    Advanced in Myofibrillar Myopathy
    Advanced in Myofibrillar Myopathy
    Saint Petersburg, SPE, RU 

    Natalia Smolina practices practicing medicine in Saint Petersburg, Russian Federation. Ms. Smolina is rated as an Advanced expert by MediFind in the treatment of Myofibrillar Myopathy. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Restrictive Cardiomyopathy (RCM), Myofibrillar Myopathy, Emery-Dreifuss Muscular Dystrophy, and Cardiomyopathy.

    Experienced in Myofibrillar Myopathy
    Experienced in Myofibrillar Myopathy
    2, Akkuratova Street, 197341, 
    Saint Petersburg, SPE, RU 

    Anna Zlotina practices practicing medicine in Saint Petersburg, Russian Federation. Ms. Zlotina is rated as an Experienced expert by MediFind in the treatment of Myofibrillar Myopathy. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Emery-Dreifuss Muscular Dystrophy, Restrictive Cardiomyopathy (RCM), Ulnar-Mammary Syndrome, and Familial Progressive Cardiac Conduction Defect.

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    Experienced in Myofibrillar Myopathy
    Experienced in Myofibrillar Myopathy
    Saint Petersburg, SPE, RU 

    Kirill Kondratov practices practicing medicine in Saint Petersburg, Russian Federation. Mr. Kondratov is rated as an Experienced expert by MediFind in the treatment of Myofibrillar Myopathy. His clinical expertise encompasses Myofibrillar Myopathy.

    Experienced in Myofibrillar Myopathy
    Experienced in Myofibrillar Myopathy
    Saint Petersburg, SPE, RU 

    Aleksandr Khudiakov practices practicing medicine in Saint Petersburg, Russian Federation. Mr. Khudiakov is rated as an Experienced expert by MediFind in the treatment of Myofibrillar Myopathy. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Familial Progressive Cardiac Conduction Defect, Emery-Dreifuss Muscular Dystrophy, Restrictive Cardiomyopathy (RCM), and Cardiomyopathy.

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
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    Last Updated: 04/28/2026

    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.