What is post-streptococcal glomerulonephritis?
Type of glomerulonephritis that occurs 1-2 weeks after a URTI and sore throat - causes haematuria, oliguria, oedema, hypertension, variable proteinuria and abnormal renal function
What are the causes of acute glomerulonephritis?
(6)
What investigations should be done for suspected post-strep glomerulonephritis?
(4)
What is the management of post-streptococcal glomerulonephritis?
(4)
What is Alport Syndrome?
Genetic condition caused by mutations in the COL4A(3/4/5) genes resulting in abnormal type IV collagen affecting ears/eyes and kidneys
What age group does Alport Syndrome tend to present in?
Infancy/teenage years
- this is because type IV collagen subunit 3,4 and 5 only form in this age group (it’s subunits 1 and 2 that are present in babies)
What are the presenting features of Alport syndrome?
Kidney - microscopic (progressing to gross) haematuria +/- proteinuria
Eyes - myopia, nearsightedness, lens opacification
Ears - sensioneural hearing loss
How is the diagnosis of Alport syndrome confirmed?
Kidney or skin biopsy sent for immunohistochemistry
What is the management of Alport syndrome?
(3)
Kidney - ACE inhibitors; or dialysis/transplant if severe
Eyes - replacement lens for anterior lenticonus
How do you differentiate between cranial DI and nephrogenic DI?
When desmopressin is given:
- if there is no response to urine osmolality (ie. kidneys still aren’t able to concentrate urine) = nephrogenic DI
- if there is a response to urine osmolality = cranial DI
What are the indications for albumin infusion in nephrotic syndrome?
Symptomatic hypovolaemia (eg CRT 5secs)
Severe diuretic-resistant oedema