18 November 2022
: Case report
A 6-Day-Old Male Infant with Severe Hyperbilirubinemia Diagnosed with Hereditary Spherocytosis at a Tertiary Hospital in East Java, Indonesia: A Diagnostic and Management Challenge in a Developing Country
Challenging differential diagnosis, Unusual setting of medical care, Rare disease
Brigitta I.R.V. Corebima





DOI: 10.12659/AJCR.937416
Am J Case Rep 2022; 23:e937416
Table 1. Patient’s laboratory examination results.The patient’s laboratory examination results show normal results of liver and renal function tests, serum electrolytes, and also marker of infection.
Laboratory examination | Patient’s results | Reference value |
---|---|---|
AST | 26 | 0–40 U/L |
ALT | 7 | 0–41 U/L |
Albumin | 3.71 | 3.5–5.5 g/dL |
Urea | 25.1 | 16.6–48.5 mg/dL |
Creatinine | 0.41 | <1.2 mg/dL |
Sodium | 140 | 136–145 mmol/L |
Potassium | 4.61 | 3.5–5 mmol/L |
Chloride | 104 | 98–106 mmol/L |
Calcium | 7.9 | 7.6–11 mg/dL |
Procalcitonin | 0.26 | <0.5 ng/mL |
Blood culture | Sterile | Sterile |