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Table 1 Results of laboratory examination at diagnosis

From: An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case report

WBC

6.01 × 109/L

PTINR

1.08

TP

53 g/L

Ferr

420 µg/L

Neut

0.84 × 109/L

APTT

34.5 seconds

ALB

41 g/L

Fe

51 µmol/L

Lymp

4.99 × 109/L

Fib

0.8 g/L

T-Bil

58 µmol/L

UIBC

4.7 µmol/L

  

D-d

5340 µg/L

D-Bil

5.1 µmol/L

TIBC

56 µmol/L

RBC

1.73 × 1012/L

ATIII

76%

AST

70 U/L

  

Hb

52 g/L

  

ALT

34 U/L

Folate

< 0.9 nmol/L

MCV

84.4 fL

  

LDH

1728 U/L

Vit.B12

31 pmol/L

MCH

30 pg

C3

0.6 g/L

BUN

3.9 mmol/L

Hp

< 0.10 g/L

MCHC

360 g/L

C4

0.2 g/L

Cre

22 µmol/L

Direct Coombs

(–)

Ht

0.146 fraction

CH50

5740 U/L

Na

138 mmol/L

Indirect Coombs

(–)

Plt

37 × 109/L

  

K

5.0 mmol/L

O157 LPS Ab

(–)

Ret

4.8 × 109/L

IgG

2.58 g/L

Cl

105 mmol/L

ADAMTS13

0.989 IU/mL

Schistocyte

138 × 109/L

IgA

0.09 g/L

Ca

2.32 mmol/L

  
  

IgM

0.09 g/L

IP

1.32 mmol/L

  
    

CRP

< 1.0 mg/L

  
  1. WBC white blood cell, Neut neutrophil, lymp lymphocyte, RBC red blood cell, Hb hemoglobin, MCV mean corpuscular volume, MCH mean corpuscular hemoglobin, MCHC mean corpuscular hemoglobin concentration, Ht hematocrit, Plt platelet, Ret reticulocyte, PTINR international normalized ratio of prothrombin time, APTT activated partial thromboplastin time, Fib fibrinogen, D-d D-dimer, ATIII antithrombin, C3 complement component 3, C4 complement component 4, CH50 50% hemolytic unit of complement, IgG Immunoglobulin G, IgA Immunoglobulin A, IgM Immunoglobulin M, TP total protein, ALB albumin, T-Bil total bilirubin, D-Bil direct bilirubin, AST aspartate aminotransferase, ALT alanine aminotransferase, LDH lactate dehydrogenase, BUN blood urea nitrogen, Cre creatinine, Na sodium, K potassium, Cl chloride, Ca calcium, IP inorganic phosphorus, CRP C-reactive protein, Ferr ferritin, Fe ferrum, UIBC unsaturated iron binding capacity, TIBC total iron binding capacity, Vit.B12 Vitamin B12, Hp haptoglobin, O157 LPS Ab O157 lipopolysaccharide antibody, ADAMTS13 a disintegrin-like and metalloproteinase with thrombospondin type 1 motifs 13