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. 2017 Jun 6;7(5):e014821. doi: 10.1136/bmjopen-2016-014821

Table 1.

Patient demographics

Variable n (%)
Gender
  Male 22 (58%)
  Female 16 (42%)
Age group (years)
  4–10 18 (47%)
  11–15 9 (24%)
  16–18 11 (29%)
Primary diagnosis
  Hereditary
  Renal dysplasia 11 (31%)
  Metabolic disorders 5 (14%)
  Nephronophthisis 2 (6%)
  Autosomal recessive polycystic kidney disease 2 (6%)
  Autosomal dominant polycystic kidney disease 1 (3%)
  Congenital nephrotic syndrome 1 (3%)
  Alport syndrome 1 (3%)
  Acquired
  Reflux nephropathy 4 (11%)
  Haemolytic uremic syndrome 3 (8%)
  Glomerulonephritis/focal segmental glomerulosclerosis 3 (8%)
  Tubulopathy 2 (6%)
  Ischaemic renal Injury 1 (3%)
Kidney transplant
  Yes 13 (36%)
  No 23 (64%)