Two families with hereditary renal amyloidosis were found to have a novel mutation in the fibrinogen Aa chain gene. This form of amyloidosis is an autosomal dominant condition char- acterized by proteinuria, hypertension, and subsequent azotemia.
No takes yet. Share an insight, caveat, or question.
Uemichi et al. (1994) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: