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Table 1 Laboratory test results

From: Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq)

 

Tests

At diagnosis

At 18 months follow up

Normal

Urine

Total protein

715.7 mg/24 h

709 mg/24 h

< 150 mg/24 h

Total LMWP

1270 mg/L

  

β2M

25.77 mg/L

 

0–0.3 mg/L

α1M

284.47 mg/L

 

< 12 mg/L

Microalbumin

245.3 mg/L

 

< 30 mg/L

IgG

41.8 mg/L

 

< 10 mg/L

Transferrin

28.3 mg/L

 

< 2.4 mg/L

RBP

13.7 mg/L

 

< 0.5 mg/L

Calcium

81.2, 90.6 mg/24 ha

93 mg/24 h

100–300 mg/24 h

Calcium/creatinine ratio

0.40, 0.46a

0.37

< 0.14

Blood

Calcium

2.16 mmol/L

2.37 mmol/L

2.2–2.65 mmol/L

Creatinine

38 μmol/L

43 μmol/L

~  44–133 μmol/L

Phosphorus

1.25 mmol/L

1.2 mmol/L

1.29–2.26 mmol/L

25(OH)D

21.8 nmol/L

18.4 nmol/L

50–125 nmol/L

BAP

< 200

 

~  12.1–42.7

Peak level of GH

6.4 ng/ml

 

> 10 ng/ml

LH

1.03 IU/L

 

< 0.4 IU/L

FSH

36.6 IU/L

 

0.5–3.2 IU/L

E2

100 pmol/L

 

< 149.2 pmol/L

  1. 25(OH) D 25-hydroxy vitamin D, BAP Bone-specific alkaline phosphatase, E2 Estradiol, FSH Follicle-stimulating hormone, GH Growth hormone, IgG Immunoglobulin G, LH Lutenizing hormone, LMWP Low molecular weight protamine, RBP Retinol binding protein, α1M α-1-microglobulin, β2M β-2-microglobulin
  2. aResults for the two tests