| HFRS | Hemorrhagic Fever with Renal Syndrome [HP 849-50] = Korean Hemorrhagic Fever &nbs... |
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| MGN | Membranous Glomerulo-Nephritis(Nephropathy) |
| MPGN | Mesangial(Membrano-) Proliferative Glomerulo-Nephritis |
| PN | 1) Pyelo-Nephritis 2) Practical Nurse; 준간호사(準看護師) |
| PSGN | Post-Streptococcal Glomerulo-Nephritis |
| haemorrhagic nephritis | Acute glomerulonephritis accompanied by haematuria. (05 Mar 2000) |
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| salt-losing nephritis | A rare disorder resulting from renal tubular damage of a variety of aetiologies; mimics adrenocortical insufficiency in that abnormal renal loss of sodium chloride occurs, accompanied by hyponatraemia, azotemia, acidosis, dehydration, and vascular collapse. Synonym: salt-losing syndrome, Thorn's syndrome. (05 Mar 2000) |
| hereditary nephritis | <pathology> An inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected. This genetic disease is uncommon. Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision. Inheritance: sex-linked autosomal dominant. Incidence: 1 in 50,000. (27 Sep 1997) |
| scarlatinal nephritis | Acute glomerulonephritis occurring as a complication of scarlet fever. (05 Mar 2000) |
| serum nephritis | Glomerulonephritis occurring in serum sickness or in animals injected with foreign serum protein. (05 Mar 2000) |
| nephritis | <nephrology> Inflammation of the kidney, a focal or diffuse proliferative or destructive process which may involve the glomerulus, tubule or interstitial renal tissue. Origin: Gr. Nephros = kidney (18 Nov 1997) |
| nephritis gravidarum | Nephritis developing in pregnancy. (05 Mar 2000) |
| nephritis, hereditary | Hereditary disease characterised initially by haematuria and slowly progressing to renal insufficiency. It is sometimes associated with perceptual deafness and/or congenital ocular defects. (12 Dec 1998) |
| nephritis, interstitial | Primary or secondary disease of the renal interstitial tissue resulting from arterial, arteriolar, glomerular, or tubular disease which destroys individual nephrons, or from toxic involvement of interstitital cells and tubules due to systemic diseases such as gout, to drug exposure, or to mercury poisoning. Clinically it may be manifested primarily by loss of concentrating capacity, mineral wasting, proteinuria, and abnormal urine sediment. It may be seen in an acute form, particularly after specific bacterial infection, and may result in acute papillary necrosis. More commonly, the process is a chronic one with progressive renal atrophy and diminution of renal function. (12 Dec 1998) |
| subacute nephritis | Undesirable term for glomerulonephritis with proteinuria, haematuria and azotemia persisting for many weeks; renal changes are variable, including those of rapidly progressive and membranoproliferative glomerulonephritis. Synonym: subacute nephritis. (05 Mar 2000) |
| suppurative nephritis | Focal glomerulonephritis with abscess formation in the kidney. (05 Mar 2000) |
| syphilitic nephritis | A rare complication of congenital and secondary syphilis, with the nephrotic syndrome, resulting from glomerular immune-complex deposits. (05 Mar 2000) |
| immune complex nephritis | An immune complex disease resulting from glomerular deposits, as in systemic lupus erythematosus. (05 Mar 2000) |
| interstitial nephritis | <nephrology> A relatively uncommon condition which is characterised by inflammation of the renal tubules, glomeruli and surrounding tissue. Interstitial nephritis is usually be temporary and often associated with the use of a particular medication. Chronic and progressive forms do exist. Drugs that have been associated with interstitial nephritis include penicillins, ampicillin, sulpha drugs, non-steroidal anti-inflammatory agents, furosemide and thiazide diuretics. May result in mild kidney dysfunction or acute renal failure. Treatment may be with corticosteroids. Incidence: 1 in 25,000. (27 Sep 1997) |
| Ellis type 1 nephritis | An obsolete designation for glomerulonephritis presenting as acute glomerulonephritis, followed by complete recovery in most cases, or the development of rapidly progressive glomerulonephritis, or incomplete remission with persistent proteinuria and subsequent development of chronic glomerulonephritis. Synonym: Ellis type 1 nephritis. (05 Mar 2000) |