Amyloidosis history and symptoms

Amyloidosis Microchapters
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Classification • Primary amyloidosis • Secondary amyloidosis • Familial amyloidosis • Wild-type (senile) amyloidosis • Cardiac amyloidosis • Beta-2 microglobulin related amyloidosis • Gelsolin related amyloidosis • Lysozyme amyloid related amyloidosis • Leucocyte cell-derived chemotaxin 2 related amyloidosis • Fibrinogen A alpha-chain associated amyloidosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Overview

Symptoms depend upon the organs that are affected by the amyloid deposits. These organs can include the intestines, skeletal muscles, smooth muscles, nerves, skin, ligaments, heart, liver, spleen, and kidneys.

Symptoms

Common Symptoms

Symptoms depend on the organs affected by the deposits. These organs can include the tongue, intestines, skeletal and smooth muscles, nerves, skin, ligaments, heart, liver, spleen, and kidneys.

Symptoms include:

• Palpitations
• Hemoptysis
• Cough
• Lightheadedness
• Fatigue
• Numbness of hands and feet
• Shortness of breath
• Skin changes
• Swallowing problems
• Enlarged tongue
• Swelling in the arms and legs
• Weak hand grip
• Weight loss

Less Common Symptoms

• Decreased urine output
• Diarrhea
• Hoarseness or changing voice
• Joint pain
• Weakness