The 20 Best Mitochondrial Complex 3 Deficiency Doctors Near Me in canton, GA

Find the Top Mitochondrial Complex 3 Deficiency Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Mitochondrial Complex 3 Deficiency near canton, GA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Mitochondrial Complex 3 Deficiency
    Family Medicine
    Experienced in Mitochondrial Complex 3 Deficiency
    Family Medicine

    Canton Family Health Center

    220 Oakside Ln, 
    Canton, GA 
     (0.7 miles away)
    Languages Spoken:
    English, Spanish
    Accepting New Patients
    Offers Telehealth

    Lee Battle-Iii is a primary care provider, practicing in Family Medicine in Canton, Georgia. Dr. Battle-Iii is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Complex 3 Deficiency. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Hypertension, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Maturity Onset Diabetes of the Young. Dr. Battle-Iii is currently accepting new patients.

    Experienced in Mitochondrial Complex 3 Deficiency
    Experienced in Mitochondrial Complex 3 Deficiency
    Referral may be required

    Laureate Medical Group At Northside LLC

    470 Northside Cherokee Blvd Ste 490, 
    Canton, GA 
     (1.5 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Gavin Brown is a Neurologist practicing medicine in Canton, Georgia. Dr. Brown is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Complex 3 Deficiency. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Migraine, Neuralgia, and Chronic Inflammatory Demyelinating Polyneuropathy. Dr. Brown is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Mitochondrial Complex 3 Deficiency?

    Mitochondrial complex III deficiency is one of several conditions caused by dysfunction of mitochondria, which are specialized compartments in cells that generate more than 90% of the energy required by the body. It is a severe, multisystem disorder that includes features such as lactic acidosis, hypotonia, hypoglycemia, failure to thrive, encephalopathy, and delayed psychomotor development. Involvement of internal organs, including liver disease and renal tubulopathy, may also occur. Symptoms typically begin at birth. It is generally caused by genetic changes in nuclear DNA in the BCS1L, UQCRB and UQCRQ genes and inherited in an autosomal recessive manner. However, it may also be caused by genetic changes in mitochondrial DNA in the MTCYB gene, which is passed down maternally or occurs sporadically and may result in a milder form of the condition.
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