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Table 1 Clinical features of 12 children with CNS

From: Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

Case Age onset Birth history Weight of placenta First symptom Proteinuria
(g/m2/24 h)
Serum albumin
(g/l)
Age to ESRD FH ES
Parity GA(w) BW(g) Delivery
1 At birth G1P1 32 2400 C-sect > 25% BW Oedema 6.87 12.30 NA No No
2 13 D G1P1 33 2450 C-sect Normal Oedema 8.74 8.26 NA No No
3 3 D G1P1 37+ 2 2700 C-sect Normal Oedema 8.28 9.85 NA No No
4 1.5 M G1P1 38 NA NA Normal Oedema 6.32 12.8 NA No No
5 At birth G2P1 37+ 4 3210 C-sect Normal Oedema 7.96 8.92 3 y No No
6 At birth G2P1 NA 2760 N-labor Normal Oedema 7.58 10.20 NA No No
7 At birth G1P1 38+ 4 3100 C-sect Normal Oedema 6.92 10.50 NA No No
8 15 D G1P1 39 2850 C-sect Normal Oedema 2.88 28.20 NA No No
9 At birth G1P1 38+ 5 3100 C-sect Normal Oedema 8.63 9.65 NA No No
10 1 M G2P1 37+ 2 2880 N-labor Normal Oedema 7.89 11.20 NA No No
11 At birth G2P1 36 2700 C-sect Normal Oedema 6.28 20.1 10 m No No
12 2 M G1P1 38 1700 N-labor Normal Oedema 3.28 22.5 CKD-1 No Yes
  1. NA not available, BW Birthweight, GA Gestational age, PW Placental weight, C-sect Caesarean section, N-labour natural labour, FH Family history, ES Extrarenal symptom, CKD-1 Chronic kidney disease stage 1,