The 20 Best Behr Syndrome Doctors Near Me in gardnerville, NV

Find the Top Behr Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Behr Syndrome near gardnerville, NV. Of these, 2 are Experienced.

Location
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2 providers found
    Experienced in Behr Syndrome
    Family Medicine
    Experienced in Behr Syndrome
    Family Medicine

    Carson Valley Medical Center

    1516 Virginia Ranch Rd, 
    Gardnerville, NV 
     (2.2 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Garrett Schwartz is a primary care provider, practicing in Family Medicine in Gardnerville, Nevada. Dr. Schwartz is rated as an Experienced provider by MediFind in the treatment of Behr Syndrome. He is also highly rated in 17 other conditions, according to our data. His clinical expertise encompasses Movement Disorders, Parkinson's Disease, Infant Hyperglycemia, and Glucocorticoid-Remediable Aldosteronism. Dr. Schwartz is board certified in American Board Of Internal Medicine. Dr. Schwartz is currently accepting new patients.

    Experienced in Behr Syndrome
    Internal Medicine
    Experienced in Behr Syndrome
    Internal Medicine

    Geriatric Specialty Care Of Nevada

    1189 Kimmerling Rd, 
    Gardnerville, NV 
     (3.3 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Randolph Clark is a primary care provider, practicing in Internal Medicine in Gardnerville, Nevada. Dr. Clark is rated as an Experienced provider by MediFind in the treatment of Behr Syndrome. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Cellulitis, Dementia, Peptic Ulcer, and Alcoholic Neuropathy. Dr. Clark is board certified in American Board Of Internal Medicine. Dr. Clark is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Behr Syndrome?

    Behr syndrome is a disorder characterized by early-onset optic atrophy along with neurological features, including ataxia, spasticity, and intellectual disability. Other signs and symptoms may be present and vary from person to person. This condition is caused by genetic changes in the OPA1 gene. It is inherited in an autosomal recessive manner.