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Published on: March 14, 2017
Neonatal primary hyperparathyroidism masked by vitamin D deficiency
K Meeran1, M Husain, M Puccini
1Division of Endocrinology and Metabolism, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Insights
Neonatal primary hyperparathyroidism is a severe condition. This case study details a unique infant survival beyond three months without surgery, with hypercalcaemia masked by vitamin D deficiency.
Area of Science:
- Pediatric Endocrinology
- Metabolic Bone Disease
Background:
- Neonatal primary hyperparathyroidism (NPH) is a rare, severe disorder.
- It presents with hypercalcaemia, hypotonia, bone demineralization, fractures, and respiratory distress.
- Mortality is high without parathyroidectomy by three months of age.
Abstract:
Neonatal primary hyperparathyroidism is a life threatening disorder that is associated with severe hypercalcaemia, hypotonia, bone demineralization, fractures and respiratory distress. Treatment consists of total parathyroidectomy and without this affected infants will usually die by the age of three months. We report a patient with neonatal primary hyperparathyroidism who survived without fractures or parathyroidectomy to an age of nine months, and in whom the hypercalcaemia became masked by vitamin D deficiency. At surgery, four-gland hyperplasia was demonstrated and total parathyroidectomy followed by oral calcitriol treatment has restored well-being and normocalcaemia. An absence of skeletal complications, a survival beyond three months of age without parathyroidectomy and the masking of the hypercalcaemia by vitamin D deficiency represents a unique combination of metabolic abnormalities in a patient with neonatal primary hyperparathyroidism.
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