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Diagnosing C3G

Diagnosing C3G

Your physician will perform a number of tests in order to establish a diagnosis.

These may include:

  • Full blood count – this is to look at the level of substances such as platelets and haemoglobin in your blood. 
  • Urea & Electrolytes –this assesses your kidney function. 
  • Complement studies – to measure the levels of complement proteins C3 & C4 in your blood and to look for the presence of autoantibodies to complement proteins. 
  • Genetic testing – to see if you carry any of the known genetic faults associated with C3G. 
  • Urinalysis – looks for evidence of blood and protein in your urine that can indicate kidney damage. 
  • Ultrasound - a non-invasive scan that provides a general outline of the size and shape of your kidneys. 
  • Biopsy – a small piece of kidney tissue is removed and looked at under a microscope. This provides a more accurate picture of what may be causing the damage to the kidney. 
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