The 20 Best Cerebrotendinous Xanthomatosis Doctors Near Me in fort benton, MT

Find the Top Cerebrotendinous Xanthomatosis Experts and Specialists

Last Updated: 09/26/2026

Save doctors for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Already have a doctor?
Find A Second Opinion

MediFind found 1 doctor with experience in Cerebrotendinous Xanthomatosis near fort benton, MT. Of these, 1 are Experienced.

Location
LocationClose
1 provider found
    Experienced in Cerebrotendinous Xanthomatosis
    Family Medicine
    Experienced in Cerebrotendinous Xanthomatosis
    Family Medicine

    Benton Medical Center

    1203 15th St, 
    Fort Benton, MT 
     (1.2 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Jace Bird is a primary care provider, practicing in Family Medicine in Fort Benton, Montana. Dr. Bird is rated as an Experienced provider by MediFind in the treatment of Cerebrotendinous Xanthomatosis. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Dehydration, Alzheimer's Disease, Maturity Onset Diabetes of the Young, and Chronic Cough. Dr. Bird is currently accepting new patients.

    Learn about our expert tiers
    Showing 1-1 of 1

    Last Updated: 09/26/2026

    What is the definition of Cerebrotendinous Xanthomatosis?

    Cerebrotendinous xanthomatosis is a disorder characterized by abnormal storage of fats (lipids) in many areas of the body (lipid storage disease). People with this disorder cannot break down certain lipids effectively (such as cholesterol), so these fats form fatty yellow nodules called xanthomas, that accumulate in the body, especially in the brain and the tendons that attach muscle to bone, which is reflected in the condition name (cerebro- meaning brain and -tendinous referring to tendons). Symptoms may include diarrhea, clouding of the lens of the eyes (cataracts), tendon problems and progressive neurologic problems, such as epilepsy, movement disorders, impaired speech (dysarthria), loss of sensation in the arms and legs (peripheral neuropathy), dementia, hallucinations, and depression. Other symptoms may include brittle bones that are prone to fracture (osteoporosis) and an increased risk of developing heart or lung failure because of lipid buildup. It is caused by genetic changes in the CYP27A1 gene.