From: Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report
Laboratory test | Reference ranges and units | Values* |
---|---|---|
Lactic Acid | 0.5–2.2 mmol/L | 1.5 |
Vitamin D 25-OH | 30.0–100.0 ng/mL | 21.0* |
Creatine kinase | 20–200 U/L | 133 |
TSH | 0.50–6.90 u[IU]/mL | 2.40 |
Comprehensive metabolic panel | ||
 Glucose | 60–99 mg/dL | 95 |
 BUN | 5–18 mg/dL | 10 |
 Creatinine | 0.31–0.47 mg/dL | 0.29* |
 Calcium | 8.8–10.8 mg/dL | 9.6 |
 Sodium | 135–145 meq/L | 140 |
 Potassium | 3.4–5.1 meq/L | 4.0 |
 Chloride | 97–108 meq/L | 105 |
 CO2 | 20–28 meq/L | 25 |
 Anion gap | 5–19 meq/L | 10 |
 Albumin | 3.8–5.4 g/dL | 4.4 |
 Bilirubin, total | 0–1.2 mg/dL | 0.5 |
 Alkaline phosphatase | 0–280 U/L | 396* |
 Protein, total | 6–8 g/dL | 6.7 |
 ALT (SGPT) | 0–41 U/L | 11 |
 AST (SGOT) | 0–50 U/L | 26 |
CBC with automated differential | Â | Â |
 WBC | 5.5–15.5 10*3/uL | 8.88 |
 RBC | 3.8–5 10*6/uL | 4.45 |
 HGB | 11–14 g/dL | 12.7 |
 HCT | 33–42% | 36.8 |
 MCV | 70–87 fL | 82.7 |
 MCH | 24–31 pg | 28.5 |
 MCHC | 31–37 g/dL | 34.5 |
 RDW-SD | 36–51 fL | 36.9 |
 RDW-CV | 11.6–14.2% | 12.2 |
 NRBCS % AUTOMATED | % | 0.0 |
 NRBCS # AUTOMATED | 0–0.1 10*3 uL | < 0.01 |
 MPV | 9.2–12.8 fL | 9.4 |
 PLT | 130–450 10*3/uL | 262 |
 Neutrophils # | 1.5–8.5 10*3/uL | 5.82 |
 Lymphocytes # | 2–9 10*3/uL | 2.51 |
 Monocyte # | 0.21–1.95 10*3/uL | 0.45 |
 Eosinophils # | 0–0.45 10*3 uL | 0.07 |
 Basophils # | 0–0.22 10*3 uL | 0.01 |
 Immature Granulocyte # | 0–0.04 10*3 uL | 0.02 |
 Neutrophils % |  | 65.5 |
 Lymphocytes % |  | 28.3 |
 Monocytes % |  | 5.1 |
 Eosinophils % |  | 0.8 |
 Basophils % |  | 0.1 |
 Immature granulocyte % |  | 0.2 |