Hereditary amyloidosis
Hereditary amyloidosis: Introduction
Hereditary amyloidosis: An inherited form of amyloidosis which is characterized by a build up of the protein amyloid in tissues and organs. This form of amyloidosis tends to affect mainly the nervous system and gastrointestinal tract. Symptoms are determined by the size and location of the amyloid deposits.
More detailed information about the symptoms,
causes, and treatments of Hereditary amyloidosis is available below.
Symptoms of Hereditary amyloidosis
See full list of 22
symptoms of Hereditary amyloidosis
Wrongly Diagnosed with Hereditary amyloidosis?
Hereditary amyloidosis: Complications
Review possible medical complications related to Hereditary amyloidosis:
Causes of Hereditary amyloidosis
Read more about causes of Hereditary amyloidosis.
Evidence Based Medicine Research for Hereditary amyloidosis
Medical research articles related to Hereditary amyloidosis include:
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Research about Hereditary amyloidosis
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Statistics for Hereditary amyloidosis
Hereditary amyloidosis: Broader Related Topics
Types of Hereditary amyloidosis
User Interactive Forums
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Definitions of Hereditary amyloidosis:
Hereditary amyloidosis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hereditary amyloidosis, or a subtype of Hereditary amyloidosis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Contents for Hereditary amyloidosis: