The 20 Best Familial Transthyretin Amyloidosis Doctors Near Me in des moines, IA

Find the Top Familial Transthyretin Amyloidosis 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 Familial Transthyretin Amyloidosis near des moines, IA. Of these, 1 are Experienced.

Location
LocationClose
1 provider found
    Experienced in Familial Transthyretin Amyloidosis
    Experienced in Familial Transthyretin Amyloidosis
    Referral may be required

    MercyOne Iowa Heart Center Des Moines

    411 Laurel St., Suite A250, 
    Des Moines, IA 
     (0.7 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Akrivi Manola is a Cardiologist practicing medicine in Des Moines, Iowa. Dr. Manola is rated as an Experienced provider by MediFind in the treatment of Familial Transthyretin Amyloidosis. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Heart Failure, Pulmonary Edema, Heart Failure with Preserved Ejection Fraction (HFpEF), and Cardiomyopathy. Dr. Manola 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 Familial Transthyretin Amyloidosis?

    Familial transthyretin amyloidosis (FTA) is a rare inherited condition characterized by abnormal build-up of a protein called amyloid in the body's organs and tissues. Signs and symptoms depend on where the amyloid protein is building up. Amyloid build-up in the nerves of the peripheral nervous system causes a loss of sensation in the lower limbs, feet, and hands (peripheral neuropathy). Amyloid build-up can also affect the involuntary body functions, such as blood pressure, heart rate, and digestion. Other areas of the body that may be affected are the heart, kidneys, eyes, and gastrointestinal tract. FTA is caused by changes in the TTR gene. Inheritance is autosomal dominant, but not all people with a TTR genetic change will develop FTA. Diagnosis of FTA is suspected by signs and symptoms and confirmed by tissue biopsy and genetic testing.
    15 miles has been selected.