Skip to main content
. 2019 Feb 26;35(3):390–397. doi: 10.1093/ndt/gfz028

Table 1.

Frequency of clinical diagnostic subgroups in patients with childhood-onset ESKD versus adult-onset ESKD

Diagnostic group Childhood-onset ESKDa
Adult-onset ESKDb
N % N %
CAKUT (39) NR
Aplasia/hypoplasia/dysplasia 1769 16
Obstructive uropathy 1713 15
Reflux nephropathy 576 5
Prune belly 279 2
Glomerulonephritis 1845 16 8802 8
FSGS 1308 12
Congenital nephrotic syndrome 289 3
Membranous nephropathy 51 <1
Cystic kidney disease 2482 2
PKD 339 3
Medullary cystic kidney disease 305 3
Cystinosis 225 2 NR
Oxalosis 58 1 NR
Renal infarct 144 1 NR
Diabetic nephropathy 11 <1 51 339 44
Hypertension 0 0 33 585 29
Other/unknown 2270 20 20 782 18
Total 11 182 100 116 990 100

Note that where there is a much higher occurrence of CAKUT (39%) in childhood-onset disease, diabetic nephropathy (44%) and hypertensive nephropathy (29%) predominate in adult-onset disease.

a

Adapted from Contributions of the Transplant Registry: The 2014 Annual Report of the North American Pediatric Renal Trials and Collaborative Studies, https://web.emmes.com/study/ped/annlrept/annualrept2014.pdf (8 February 2019, date last accessed).

b

Adapted from the 2015 United States Renal Data System Annual Data Report detailing the primary cause of ESRD in incident cases of hemodialysis, peritoneal dialysis and transplantation in the US population, https://www.usrds.org/2015/download/vol2_USRDS_ESRD_15.pdf (8 February 2019, date last accessed).

NR, not reported; PKD, polycystic kidney disease.