The 20 Best Olivopontocerebellar Atrophy Doctors Near Me in jonesboro, AR

Find the Top Olivopontocerebellar Atrophy Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Olivopontocerebellar Atrophy near jonesboro, AR. Of these, 2 are Experienced.

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2 providers found
    Experienced in Olivopontocerebellar Atrophy
    Internal Medicine
    Experienced in Olivopontocerebellar Atrophy
    Internal Medicine

    St Bernards Clinics Inc

    300 Carson St, 
    Jonesboro, AR 
     (0.4 miles away)
    Languages Spoken:
    English

    Ben Owens is a primary care provider, practicing in Internal Medicine in Jonesboro, Arkansas. Dr. Owens is rated as an Experienced provider by MediFind in the treatment of Olivopontocerebellar Atrophy. He is also highly rated in 153 other conditions, according to our data. His clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Hypertension, Familial Hypertension, Endoscopy, and Gastrostomy.

    Experienced in Olivopontocerebellar Atrophy
    Internal Medicine
    Experienced in Olivopontocerebellar Atrophy
    Internal Medicine

    Encompass Health Rehabilitation Hospital Of Jonesboro

    1201 Fleming Ave, 
    Jonesboro, AR 
     (0.7 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Gerald Stipanuk is a primary care provider, practicing in Internal Medicine in Jonesboro, Arkansas. Dr. Stipanuk is rated as an Experienced provider by MediFind in the treatment of Olivopontocerebellar Atrophy. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Necrotizing Myopathy (NM), Childhood Iron Deficiency Anemia, Pneumonia, Rhabdomyolysis, and Gastrostomy. Dr. Stipanuk is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Olivopontocerebellar Atrophy?

    Olivopontocerebellar atrophy (OPCA) is a term used for a progressive condition characterized by the degeneration of nerve cells (neurons) in specific areas of the brain. OPCA can be viewed as a finding of several diseases, and indicates a form of progressive ataxia (abnormal or uncontrolled movements) distinguished by characteristic findings in brain imaging studies and at autopsy (pontine flattening and cerebellar atrophy). It was traditionally divided in hereditary or genetic OPCA and sporadic OPCA. Currently, most of the major forms of hereditary OPCA refer to disorders that overlap with spinocerebellar ataxia (SCA), which is a neurological disorder characterized by ataxia. The sporadic forms are considered now to be a form of multiple system atrophy (MSA). OPCA may also occur in people with prion disorders and inherited metabolic diseases. The main symptom is clumsiness that slowly gets worse. Other symptoms may include problems with balance; speech or swallowing problems; difficulty walking; abnormal eye movements; muscle spasms; and neuropathy. Whether OPCA is inherited (and the inheritance pattern) depends on the underlying cause, if known.

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