The 20 Best Familial Transthyretin Amyloidosis Doctors in Saudi Arabia

Find the Top Familial Transthyretin Amyloidosis Experts and Specialists

Last Updated: 06/30/2026

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MediFind found 3 doctor with experience in Familial Transthyretin Amyloidosis near Saudi Arabia. Of these, 3 are Experienced.

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3 providers found
    Experienced in Familial Transthyretin Amyloidosis
    Experienced in Familial Transthyretin Amyloidosis
    Referral may be required
    Riyadh, SA 

    Bahaa Fadel practices practicing medicine in Riyadh, Saudi Arabia. Mr. Fadel is rated as an Experienced expert by MediFind in the treatment of Familial Transthyretin Amyloidosis. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Restrictive Cardiomyopathy (RCM), Cardiac Tamponade, Aortic Regurgitation, Heart Transplant, and Angioplasty.

    Experienced in Familial Transthyretin Amyloidosis
    Experienced in Familial Transthyretin Amyloidosis
    Referral may be required
    Dammam, SA 

    Munirah Alafaleq practices practicing medicine in Dammam, Saudi Arabia. Ms. Alafaleq is rated as an Experienced expert by MediFind in the treatment of Familial Transthyretin Amyloidosis. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Hereditary Keratitis, Cat Scratch Disease, Neurotrophic Keratitis, and Neuroretinitis.

    Experienced in Familial Transthyretin Amyloidosis
    Experienced in Familial Transthyretin Amyloidosis
    Referral may be required
    Riyadh, SA 

    Omar Ahmad practices practicing medicine in Riyadh, Saudi Arabia. Mr. Ahmad is rated as an Experienced expert by MediFind in the treatment of Familial Transthyretin Amyloidosis. His clinical expertise encompasses Congenital Mitral Stenosis, Cardiac Amyloidosis, Primary Amyloidosis, and Restrictive Cardiomyopathy (RCM).

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    Last Updated: 06/30/2026

    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.
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