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. 2017 Feb 16;10(5):625–631. doi: 10.1093/ckj/sfw143

Table 1.

Laboratory findings in the three cases at admission

Case 1 Case 2 Case 3
Age (years) 46 32 34
Sex F F M
Creatinine (mg/dL) 2.2 2.15 2.97
Urea (g/L) 1.01 1.28
Urinalysis No microhaematuria No microhaematuria Microhaematuria, glycosuria
24 h proteinuria (g) 1.5 4.9 1.32
Hb (g/dL) 6.9 8.0 6.3
Platelet (per mm3) 43 000 19 000 73 000
PT, APTT, antithrombin, D-dimer Normal range Normal range Normal range
Lactate dehydrogenase (U/L) 1230 1929 1840
Coombs test Negative Negative Negative
Haptoglobine Undetectable Undetectable Undetectable
Schistocytes on peripheral blood smear (%) 7 5 3
ADAMTS-13 (%) (ref. 50 – 150%) 90 52 89
Anti-CFH antibodies Negative Negative Negative
Complement gene mutation analysis Negative (CFH, CFHR1-R3, MCP, CFI, CFB)
  • Non-pathogenic heterozygous deletion CFHR1-R3

  •    (negative CFH, MCP, CFI and CFB)

  • Non-pathogenic heterozygous MCP mutation

  •    (negative CFH, CFHR1-R3, CFI and CFB)

PT, prothrombin time; APTT, activated partial thromboplastin time.