The 20 Best Alpers-Huttenlocher Syndrome Doctors Near Me in carmichael, 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 carmichael, CA. Of these, 2 are Experienced.

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

    Office

    5810 Jameson Ct, 
    Carmichael, CA 
     (2.3 miles away)
    Experience:
    44+ years
    Languages Spoken:
    English, Russian
    Offers Telehealth

    Vladimir Rafanov is a Neurologist practicing medicine in Carmichael, California. He has been practicing medicine for over 44 years. Dr. Rafanov is rated as an Experienced provider by MediFind in the treatment of Alpers-Huttenlocher Syndrome. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Photosensitive Epilepsy, Epilepsy in Children, Infant Epilepsy with Migrant Focal Crisis, and Seizures.

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

    El Hadi Mouderres MD Inc

    9727 Elk Grove Florin Rd Ste 120, 
    Elk Grove, CA 
     (13.1 miles away)
    Languages Spoken:
    English, Arabic, French

    El-hadi Mouderres is a Neurologist practicing medicine in Elk Grove, California. Dr. Mouderres is rated as an Experienced provider by MediFind in the treatment of Alpers-Huttenlocher Syndrome. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Thromboangiitis Obliterans, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, Memory Loss, and Multiple Mononeuropathy.

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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.

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