The 20 Best Mitochondrial Complex 2 Deficiency Doctors Near Me in austin, TX

Find the Top Mitochondrial Complex 2 Deficiency Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Mitochondrial Complex 2 Deficiency near austin, TX. Of these, 1 are Advanced.

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1 provider found
    Advanced in Mitochondrial Complex 2 Deficiency
    Advanced in Mitochondrial Complex 2 Deficiency
    Referral may be required

    Dell Children's Medical Group - Neurology Pavilion

    4910 Mueller Blvd, Ste 300, 
    Austin, TX 
     (4.3 miles away)
    512-628-1855
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Vettaikorumakankav Vedanarayanan is a Pediatrics specialist and a Neurologist practicing medicine in Austin, Texas. Dr. Vedanarayanan is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Complex 2 Deficiency. He is also highly rated in 39 other conditions, according to our data. His clinical expertise encompasses Inclusion Body Myositis, Amyotonia Congenita, Congenital Myasthenic Syndrome, and Dystrophinopathy. Dr. Vedanarayanan is board certified in The American Board Of Psychiatry And Neurology - Neurology With Special Qualification In Child Neurology, The American Board Of Psychiatry And Neurology - Neuromuscular Medicine, and The American Board Of Psychiatry And Neurology - Clinical Neurophysiology. Dr. Vedanarayanan is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Mitochondrial Complex 2 Deficiency?

    Complex II deficiency is a mitochondrial disease. Mitochondria are specialized compartments in cells that create more than 90% of the energy needed by the body. In mitochondrial diseases, the mitochondria don't work correctly resulting in less energy in the cell, cell injury and cell death. The symptoms can vary greatly from serious symptoms in infancy to muscle disease beginning in adulthood. Complex II deficiency can be caused by genetic changes in the SDHA, SDHB, SDHD, or SDHAF1 genes. In many cases the underlying genetic changes cannot be identified. Complex II deficiency is inherited in an autosomal recessive fashion. Complex II deficiency genetic change carriers may be at an increased risk for certain cancers.

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