International Journal of Nephrology / 2017 / Article / Tab 5

Research Article

End-Stage Kidney Failure in Oman: An Analysis of Registry Data with an Emphasis on Congenital and Inherited Renal Diseases

Table 5

Inherited kidney diseases in ESKD population (2001–2015).

Inherited kidney diseaseNumberProportion of inherited kidney disease (%)Proportion of ESRD in this cohort (%)Age group ()
0–12 13–1920–4445+

Autosomal dominant polycystic kidney disease (ADPKD)5640.32111737
Congenital anomalies of kidney and urinary tract (CAKUT)1611.50.68620
Alport syndrome139.40.50760
Autosomal recessive polycystic kidney disease (ARPKD)107.20.43601
Dysplastic cystic kidney750.21321
Steroid resistant nephrotic syndrome (congenital & childhood)53.60.24100
Primary hyperoxaluria53.60.22210
Prune-belly syndrome53.60.22210
Familial focal segmental glomerulosclerosis53.60.21220
Medullary cystic kidney42.90.13010
Familial interstitial nephropathy21.40.11100
Haemolytic uremic syndrome21.40.12000
Mesangioproliferative glomerulosclerosis21.40.10110
Membranoproliferative glomerulosclerosis21.40.10002
Bartter syndrome10.700100
Lowe's syndrome10.700100
Renal tubular acidosis10.700100
Undetermined familial disease10.701000


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