Table 2 Clinical characteristics and disease category of patients
From: Clinical utility of genetic testing in Indian children with kidney diseases
Age in months (median, IQR) | 72 (24–120) |
Age in months at disease onset (median, IQR) | 48 (12–96) |
Sex Male | 40 (52.6%) |
Consanguinity | 7 (10.5%) |
Glomerular diseases SRNS Atypical HUS Dense deposit disease + HUS C3 GN Alport Syndrome | 34 (44.7%) 25 04 01 01 03 |
Tubular disorders Fanconi syndrome Distal RTA Bartter syndrome Rickets Low molecular weight proteinuria Unclassified | 13 (17.1%) 05 02 02 01 01 02 |
Nephrolithiasis/calcinosis Primary hyperoxaluria Nephrolithiasis with hyperuricemia FHHNC | 11 (14.4%) 08 02 01 |
Cystic kidney disease Nephronophthisis related ciliopathy Bardet Biedl Syndrome Glomerulocystic kidney disease ADPKD ARPKD | 10 (13.1%) 05 02 01 01 01 |
CKD of unknown aetiology | 04 (5.2%) |
CAKUT | 02 (2.6%) |
Others | 02 (2.6%) |
Total | 76 (100%) |