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Table 1 Initial hypoglycaemia screen and CSF results

From: The search for a unifying diagnosis involving neurological, endocrine and immune dysfunction: a case report of a novel presentation of DAVID syndrome

Parameter

Patient

Normal Range

Glucose

1.9 mmol/L

> 2.6 mmol/L

Insulin

 < 0.4mIU/L

2.6–24.9mIU/L

B-hydroxybutyrate

6.37 mmol/L

0.0–0.27 mmol/L

Free fatty acids

2.4 mEq/L

0.0–0.6 mEq/L

Cortisol

< 30 nmol/L

> 400 nmol/L

Growth hormone

14.6ug/L

> 5ug/L

Ammonia

44umol/L

0.0-70umol/L

Pyruvate

0.06 mol/L

0.0–0.18 mol/L

Amino acids

Not suggestive of metabolic disease

CSF 1: Initial presentation

WCC < 1, RBC < 1

0% polymorphonuclear cells, 5% lymphocytes, 1% monocytes

Protein 0.23, glucose 2.6

No growth, viral PCR negative

CSF 2: Eight days following presentation

WCC 2, RBC 22

8% polymorphonuclear cells, 53% lymphocytes, 39% monocytes

Protein 0.23, glucose 2.8

No growth

CSF 3: Three months following presentation

WCC 1, RBC < 1

Insufficient cells for differential

Protein 0.28, glucose 2.9

No growth

Borderline raised neopterin (31.25 nmol/L), normal amino acids, CSF IgG < 4 mg/L, Serum IgG 1.9 g/L, CSF/serum albumin index 3.3. Matching oligoclonal IgG bands present in CSF and serum

  1. WCC White cell count, RBC Red blood cell count