Avtor/Urednik		Kaplan-Pavlovčič, Staša
Naslov		Clinical presentation of renal monoclonal immunoglobulin deposition disease
Tip		članek
Vir		In: Vizjak A, Ferluga D, Bussolati G, editors. Update in pathology. Proceedings of the 19th European congress of pathology: nephropathology pre-congress meeting advances in nephrology, pulmonary pathology pre-congress meeting; 2003 Sep 6-11; Ljubljana. Ljubljana: Faculty of medicine,
Leto izdaje		2003
Obseg		str. 300-2
Jezik		eng
Abstrakt		In the retrospective study we evaluated clinical characteristics of 20 patients with nonamyloidotic monoclonal immunoglobulin deposition diseases (MIDD); light chain deposition disease (LCDD) I S patients, heavy chain deposition disease (HCDD) 3 patients and with light and heavy chain deposition disease (LHCDD) 2 patients. Patient's age ranged from 39 to 75 years, The onset of nephropathy was manifested as rapidly progressive renal failure or chronic renal failure with the concentration of serum creatinine from 200 to 533 micromo1/l. All patients had proteinuria (from 0,9 to 10 g/24 hours).
Deskriptorji		KIDNEY DISEASES IMMUNOGLOBULINS, LIGHT-CHAIN IMMUNOGLOBULINS, HEAVY-CHAIN IMMUNE COMPLEX DISEASES IGG IGA IGM IGD IMMUNOELECTROPHORESIS