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. 2022 Dec 13;5(2):100585. doi: 10.1016/j.xkme.2022.100585

Table 1.

Characteristics of Patients in the Renal Genetics Clinic at Index Visit

Factor Total (N=309)
Age (at first visit), y, mean ± SD 35.1 ± 20.3
Male, No. (%) 118 (38.2%)
White, No. (%) 232 (75.1%)
African American, No. (%) 49 (15.9%)
Family history of kidney disease, No. (%)
 Yes 163 (52.8%)
 No 143 (46.3%)
 N/A 3 (1.0%)
Presentations, No. (%)
 Glomerular disease 102 (33.0%)
 Cystic kidney disease 78 (25.2%)
 Electrolyte disorders 77 (24.9%)
 Congenital anomalies of kidneys and urinary tract 21 (6.8%)
 Kidney stones and or nephrocalcinosis 10 (3.2%)
 Living donor 9 (2.9%)
 Tubulointerstitial disease 3 (1.0%)
 Renal vascular disease 3 (1.0%)
 Family history only 5 (1.6%)
Insurance status, No. (%)
 Private 184 (59.5%)
 Medicare 50 (16.2%)
 Medicaid 64 (20.7%)
 International patient 3 (1.0%)
 Military 5 (1.60%)
 No insurance 2 (0.60%)
Kidney failure, No. (%) 33 (10.7%)
eGFRa, 60 mL/min/1.73 m2, mean ± SD 88.7 ± 45.6

Abbreviations: eGFR, estimated glomerular filtration rate; N/A, not applicable; SD, standard deviation.

a

Data not available for all subjects. eGFR in pediatric patients is calculated from the Schwartz equation based on a stable serum creatinine and height.