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Amyloid is a waxy, translucent substance that forms when normally soluble proteins misfold and create insoluble fibrous deposits. These deposits can accumulate in the connective tissues and organs of the body, interfering with normal function.12

There are different types of amyloid, distinguished by their primary protein component. Amyloidosis, the disease caused by these deposits, can be systemic, affecting multiple organs, or localized to specific areas. Organs commonly impacted include the kidneys, heart, liver, spleen, lungs, and skin. Symptoms vary based on the affected organ, ranging from gastrointestinal issues to heart failure.1

Amyloidosis can be classified as primary (occurring without an underlying disease), secondary (associated with chronic conditions like rheumatoid arthritis or tuberculosis), or hereditary (resulting from genetic mutations). A notable example is amyloid-beta protein, which forms plaques in the brain and is associated with Alzheimer's disease. Diagnosis involves detecting amyloid in bodily fluids or through tissue biopsies, with treatment focused on managing symptoms and underlying causes.123

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  1. amyloidosis
  2. amyloid
  3. amyloid beta

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