Familial renal amyloidosis is a form of amyloidosis primarily presenting in the kidney.

[1] It is associated most commonly with congenital mutations in the fibrinogen alpha chain and classified as a dysfibrinogenemia (see Hereditary Fibrinogen Aα-Chain Amyloidosis).

[2][3] and, less commonly, with congenital mutations in apolipoprotein A1[4] and lysozyme.

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