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Hereditary amyloidosis is a condition in which abnormal protein deposits (called amyloid) form in almost every tissue in the body. These protein deposits damage the tissues and interfere with the function of the involved organs.
Hereditary amyloidosis is passed down from parents to their children (inherited).
Other types of amyloidosis may be:
For further information, see the specific type:
Amyloidosis - hereditary
Updated by: Chad Haldeman-Englert, MD, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA. Review provided by VeriMed Healthcare Network.
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Page last updated: 29 October 2009 |