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Familial Amyloidosis, Finnish Type
? TBD
Medical condition
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Familial Amyloidosis, Finnish Type (FAF), also called hereditary gelsolin amyloidosis and AGel amyloidosis (AGel), is an amyloid condition with a number of associated cutaneous and neurological presentations deriving from the aberrant proteolysis of a mutated form of plasma gelsolin. First described in 1969 by the Finnish ophthalmologist Jouko...

Instance of
Genetic disorder
Rare disease
class of disease
Subclass of
Amyloidosis
Genetic disorder
Wikidata