The 20 Best Alpers-Huttenlocher Syndrome Doctors Near Me in rancho mirage, CA

Find the Top Alpers-Huttenlocher Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Alpers-Huttenlocher Syndrome near rancho mirage, CA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Alpers-Huttenlocher Syndrome
    Neurology
    Experienced in Alpers-Huttenlocher Syndrome
    Neurology
    Referral may be required

    Eisenhower Health

    39000 Bob Hope Dr, 
    Rancho Mirage, CA 
     (1.6 miles away)
    Languages Spoken:
    English

    Reza Nazemi is a Neurologist practicing medicine in Rancho Mirage, California. Dr. Nazemi is rated as an Experienced provider by MediFind in the treatment of Alpers-Huttenlocher Syndrome. He is also highly rated in 20 other conditions, according to our data. His clinical expertise encompasses Andermann Syndrome, Septic Arthritis, Tomaculous Neuropathy, and Hereditary Sensory Neuropathy Type 1 (HSN1).

    Experienced in Alpers-Huttenlocher Syndrome
    Experienced in Alpers-Huttenlocher Syndrome
    Referral may be required

    Ronald S. Levey MD Inc

    72780 Country Club Dr, 
    Rancho Mirage, CA 
     (1.7 miles away)
    Languages Spoken:
    English

    Hamid Salari-Namin is a Neurologist practicing medicine in Rancho Mirage, California. Dr. Salari-Namin is rated as an Experienced provider by MediFind in the treatment of Alpers-Huttenlocher Syndrome. He is also highly rated in 23 other conditions, according to our data. His clinical expertise encompasses Stroke, Trigeminal Neuralgia, Dysembryoplastic Neuroepithelial Tumors (DNET), and Cerebellar Degeneration.

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    Last Updated: 09/26/2026

    What is the definition of Alpers-Huttenlocher Syndrome?

    Alpers-Huttenlocher syndrome is one of the most severe of a group of conditions called the POLG-related disorders. The conditions in this group feature a range of similar signs and symptoms involving muscle-, nerve-, and brain-related functions. Alpers-Huttenlocher syndrome typically becomes apparent in children between ages 2 and 4. People with this condition usually have three characteristic features: recurrent seizures that do not improve with treatment (intractable epilepsy), loss of mental and movement abilities (psychomotor regression), and liver disease.