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Published on: December 9, 2015
[Severe hypercalcemia due to vitamin D intoxication]
C Chambellan-Tison1, B Horen, G Plat-Wilson
1POSU pédiatrique, hôpital des enfants, CHU de Toulouse, 330, avenue de Grande-Bretagne, TSA 70034, 31059 Toulouse, France.
Insights
Severe hypercalcemia in an infant was caused by vitamin D intoxication from excessive parental administration. Prompt treatment with hydration, diuretics, and biphosphonates led to full recovery, highlighting the risks of vitamin D overdose.
Area of Science:
- Pediatric Endocrinology
- Toxicology
- Clinical Case Study
Background:
- Vitamin D intoxication is a rare but serious condition in infants.
- Excessive vitamin D supplementation can lead to severe hypercalcemia.
- Cultural practices and internet accessibility of high-dose supplements contribute to this risk.
Observation:
- A 4-month-old infant presented with anorexia, weakness, hypotonia, constipation, and lethargy.
- Laboratory findings revealed severe hypercalcemia (4.28-4.55 mmol/l) and a short QTc interval on EKG.
- The infant experienced neurological deterioration, requiring transfer to the pediatric intensive care unit.
Findings:
- Diagnosis of vitamin D intoxication was confirmed due to excessive daily administration.
- Treatment involved hyperhydration, loop diuretics, and sodium pamidronate infusion.
- The infant developed nephrocalcinosis and iliac venous thrombosis but achieved full neurological recovery.
Implications:
- Vitamin D intoxication should be considered in infants with hypercalcemia and neurological symptoms, especially those with a history of excessive supplementation.
- Early diagnosis and appropriate management, including bisphosphonates, are crucial for favorable outcomes.
- Awareness of the risks associated with high-dose vitamin D supplementation is essential for parents and healthcare providers.
Unlabelled:
We report on a case of severe hypercalcemia due to vitamin D intoxication in a 4-month-old infant,
Case Report:
A 4-month-old boy was admitted for anorexia, weakness, hypotonia, constipation and lethargy. Initial physical examination evidenced a severe axial hypotonia, signs of moderate intracellular dehydration, polyuria and leucocyturia. Hemodynamic parameters were normal. The infant's origin was Turkish. Basic blood chemistry showed a high serum calcium concentration of 4.28 and 4.55 mmol/l on a second control. The EKG showed a short QTc interval calculated at 0.34 s. Due to worsening neurological condition, the infant was referred to the pediatric intensive care unit. Because of the association of neurological impairment, EKG abnormality and high serum calcium level, haemodialysis was performed. Treatment included hyperhydration, high doses of intravenous of loop diuretics and sodium pamidronate infusion. Hormonal, radiological, abdominal and cardiac investigations combined with a new parental interview led to the diagnosis of vitamin D intoxication due to excessive daily administration. We were unable to determine the exact total amount because of the language barrier. Clinical outcome was marked by nephrocalcinosis without renal function impairment, iliac venous thrombosis secondary to the dialysis catheter and a full neurological recovery without sequelae after 3 months.
Discussion:
Fear of rickets, especially in Turkish families residing in France, can lead some parents to administer massive daily quantities of vitamin D. This practice is facilitated by the possibility of purchasing high dosage forms of vitamin D via the Internet. When faced with an infant presenting with digestive disorders such as vomiting and constipation, associated with neurological troubles (lethargy, hypotonia) and hypercalcemia, vitamin D intoxication should be considered after tumoral, hormonal or malformative (Williams-Beuren syndrome) causes have been eliminated. Combined with hyperhydration and loop diuretics, biphosphonate infusion often allows to control hypercalcemia. Nephrocalcinosis seems correlated to chronic administration while cardiovascular disorders are more likely associated with massive acute vitamin D administration, severe dysrhythmia being rare in children in this context.
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