Saito T, Oikawa S, Sato H, Chiba J, Abe K
Familial occurence of lipoprotein glomerulopathy
33rd Congress of the Eur Dial Transplant Assoc
Nephrol Dial Transplant (Jun) 11:A114 1996

Lipoprotein glomerulopathy is a new glomerular disease characterized by lipoprotein thrombi and elevated plasma apolipoprotein E concentration. Investigations in the families of 3 affected patients revealed this disease is genetically determined because at least one relative of each propositus presented the same disease. Preliminary genetic studies suggest that the disease may be caused by a mutation the Apo E gene (Carmine Zoccali, M.D., Reggio Calabria, Italy).

To go back use the BACK button on your browser.
Otherwise click on the desired link to this article below:
33rd Congress of the Eur Dial Transplant Assoc
Proteinuria/Hematuria : Hereditary hematuria/proteinuria