The differences between nephrotic and nephritic syndrome are easily forgotten. At the most basic level, remember that nephrotic syndrome involves the loss of a lot of protein, whereas nephritic syndrome involves the loss of a lot of blood.

Nephrotic syndrome

Proteinurea (>3.5g in 24hrs)

++++ Protein

Urine looks frothy

Tip: Nephrotic & Protein both have an “O” which may help you remember!



Albumin is lost in the urine.

Gaps in podocytes allow proteins to leak into the urine.



Albumin is lost into the urine.

Hypoalbuminemia results in decreased intravascular oncotic pressure.

As a result fluid moves out of the intravascular compartment and into the surrounding tissues causing oedema.



Due to hypoalbuminaemia, the liver compensates and increases production, however this has the side effect of also increasing the production of lipids, hence causing hyperlipidaemia. 

Nephritic syndrome


+++ Blood –  microscopic or macroscopic haematuria

Red cell casts – distinguishing feature, form in nephrons & indicate glomerular damage

Haematuria occurs due to podocytes developing large pores which allows blood and protein to escape into the urine.



++ Protein (small amount)



Usually only mild


Low urine volume <300ml/day

Due to reduced renal function.

Differential diagnosis of Nephrotic and Nephritic syndrome

Nephrotic or nephritic syndrome can be caused by multiple disease processes . First deciding between nephritic and nephrotic syndrome is a useful starting point for your differential diagnosis. This is because each is associated with a particular subset of diseases. Below is just a quick overview of which diseases are associated with which syndrome, for more details read the Glomerulonephritis article


Nephrotic syndrome – associated diseases

Primary causes

Minimal change glomerulonephritis

Focal segmental glomerulosclerosis

Membranous glomerulonephritis.


Secondary causes


Hep B & C


Diabetes mellitus



Nephritic syndrome – associated diseases.

Post-streptococcal glomerulonephritisappears weeks after upper respiratory tract infection (URTI)

IgA nephropathyappears within a day or two after a URTI


Rapidly progressive glomerulonephritis (crescentic glomerulonephritis)

  • Goodpasture’s syndrome – anti-GBM antibodies against basal membrane antigens
  • Vasculitic disorder – Wegener’s granulomatosis / Microscopic Polyangiitis / Churg Strauss disease


Membranoproliferative glomerulonephritis primary or secondary to SLE / Hepatitis B/C

Henoch-Schönlein purpura systemic vasculitis – deposition of IgA in the skin & kidneys