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Table 1 Clinical and laboratory findings of the patient

From: A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report

Personal history

 Presenting age (months)

3.5

 Age at last following up (months)

15

 Gravidity (G) and Parity (P)

G6P2

 Gestation (weeks)

39

 Birth weight (g)

3150

 Birth history

cesarean section

Physical examination at 6.5 months old

 Head circumference (cm)

42.0

 Chest circumference (cm)

43.0

 Height (cm)

63.0

 Weight (kg)

6.8

 Temperature (°C)

37.0

 Heart rate (beats per minute)

126

 Respiration rate (times per minute)

28

 Hepatomegaly

Yes

 Splenomegaly

No

Biochemical examination

 Albumin (g/L)

45.1-50.8

 Alanine aminotransferase (IU/L)

68-110

 Aspartate aminotransferase (IU/L)

108-186

 Gammaglutamyl-transpeptidase (IU/L)

233-482

 Direct bilirubin (umol/L)

1.0-2.3

 Total bilirubin (umol/L)

2.4-9.4

 Total bile acid (umol/L)

9.0-19.8

 Alpha fetal protein (ng/mL)

53

 Triglyceride (mmol/L)

4.18-10.94

 Total cholesterol (mmol/L)

2.36-4.35

 Glucose (mmol/L)

4.2-5.7

Coagulation test

 D-dimer (mg/L)

0.27-1.18

 Activated partial thromboplastin time (s)

25.0-33.3

 Thrombin time (s)

19.4-19.9

 Prothrombin time (s)

11.0-13.3

 Fibrinogen (g/L)

1.84-1.93

Blood routine examination

 Hemoglobin (g/L)

95.0-101.0

 Red blood cell count (per liter)

4.91-5.24 × 1012

 White blood cell count (per liter)

7.7-11 × 109

 Lymphocytes (%)

65.0-75.0

 Neutrophils (%)

16.8-22.0

 Platelets count (per liter)

568-782 × 109