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
Nephronophthisis10.701000
Bartter syndrome10.700100
Lowe's syndrome10.700100
Renal tubular acidosis10.700100
Undetermined familial disease10.701000

Total139100%5%30353336

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