Heredofamilial amyloidosis

Heredofamilial amyloidosis is a type of amyloidosis that is inherited in an autosomal dominant manner. It is characterized by the deposition of amyloid (abnormal proteins) in various body tissues and organs, which can lead to a variety of symptoms and complications.

Causes[edit | edit source]

Heredofamilial amyloidosis is caused by mutations in various genes. These mutations lead to the production of abnormal proteins that form amyloid. The amyloid then deposits in various tissues and organs, causing damage and dysfunction.

Symptoms[edit | edit source]

The symptoms of heredofamilial amyloidosis can vary widely, depending on which tissues and organs are affected. They can include:

Diagnosis[edit | edit source]

The diagnosis of heredofamilial amyloidosis is based on the presence of characteristic symptoms, a family history of the disease, and the results of various tests. These tests can include:

Treatment[edit | edit source]

The treatment of heredofamilial amyloidosis is aimed at managing symptoms and slowing the progression of the disease. It can include:

Prognosis[edit | edit source]

The prognosis for individuals with heredofamilial amyloidosis can vary widely, depending on the severity of the disease and the organs affected. Some individuals may have a relatively normal lifespan, while others may have a significantly shortened lifespan due to complications of the disease.

See also[edit | edit source]

Heredofamilial amyloidosis Resources
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