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Amyloidosis



Amyloidosis: Introduction

Amyloidosis: Proteins are important building blocks for all body parts, including muscles, bones, hair, and nails. Proteins circulate throughout the body in ... more about Amyloidosis.

Amyloidosis: A rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage and is potentially fatal. Symptoms depend on the organs involved. There are numerous forms of the condition: primary amyloidosis, secondary amyloidosis, hemodialysis-associated amyloidosis and familial amyloidosis. More detailed information about the symptoms, causes, and treatments of Amyloidosis is available below.

Symptoms of Amyloidosis

See full list of 79 symptoms of Amyloidosis

Home Diagnostic Testing

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Amyloidosis: Complications

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Medical Textbooks Online about Amyloidosis

Medical Books Excerpts
  • "Professional Guide to Diseases (Eighth Edition)" (2005)

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Amyloidosis?

Misdiagnosis and Amyloidosis

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed. Women with the condition tend to have heavy periods, since they actually have a bleeding disorder. Severe afflictions may result in the women receiving a hysterectomy unnecessarily, when the underlying cause has not been identified. See the introduction to Von Willebrand's disease and bleeding disorder....read more »

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Amyloidosis: Research Doctors & Specialists

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Causes of Amyloidosis

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Patient Surveys for Amyloidosis

Prognosis for Amyloidosis

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Reseach about Amyloidosis

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Clinical Trials for Amyloidosis

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Amyloidosis include:

See full list of 71 Clinical Trials for Amyloidosis

Statistics for Amyloidosis

Amyloidosis: Broader Related Topics

Types of Amyloidosis

Types of Amyloidosis

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Stories from Users Related to Amyloidosis

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Article Excerpts about Amyloidosis

Amyloidosis and Kidney Disease: NIDDK (Excerpt)

Proteins are important building blocks for all body parts, including muscles, bones, hair, and nails. Proteins circulate throughout the body in the blood and are normally harmless. Occasionally, cells produce abnormal proteins that can settle in body tissue, forming deposits and causing disease. When these deposits of abnormal proteins were first discovered, they were called amyloid, and the disease process amyloidosis. (Source: excerpt from Amyloidosis and Kidney Disease: NIDDK)

Kidney Failure Glossary: NIDDK (Excerpt)

A condition in which a protein-like material builds up in one or more organs. This material cannot be broken down and interferes with the normal function of that organ. People who have been on dialysis for several years often develop amyloidosis because the artificial membranes used in dialysis fail to filter the protein-like material out of the blood. (Source: excerpt from Kidney Failure Glossary: NIDDK)

Definitions of Amyloidosis:

A disease characterised by the deposition of amyloid in various organs of the body. It is generally considered that the amyloidoses share common pathogenic mechanisms which lead to protein fibril formation and deposition. These mechanisms may include structural, metabolic, genetic and environmental factors that may be common to all forms of amyloidosis. Primary amyloidosis, while the most common form of amyloidosis, is a sporadic disease and, therefore, can only be investigated on a case by case basis. Secondary (reactive) amyloidosis occurs in subjects with chronic inflammatory disease or cancer but factors which predict amyloid formation and which subject is going to be affected, are not readily apparent. Alzheimer disease, while very common in the aged population, is unpredictable except for those rare forms of familial Alzheimer disease with characterized mutations in specific genes. Hereditary transthyretin amyloidosis has generally been considered a rare disease and the original impetus to study the pathogenesis of this disease was because it represented a human model of systemic amyloidosis. - (Source - Diseases Database)

A disorder characterized by deposit of amyloid in organs or tissues; often secondary to chronic rheumatoid arthritis or tuberculosis or multiple myeloma - (Source - WordNet 2.1)

Amyloidosis is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Amyloidosis, or a subtype of Amyloidosis, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Amyloidosis as a "rare disease".
Source - Orphanet


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