A challenging case of neonatal hyperparathyroidism

Vivek Aggarwal, Manish Sahni, Neeraj Gupta, Deepak Khandelwal

Thyroid Research and Practice 2017 14(3):130-132

Neonatal severe primary hyperparathyroidism (NSPHT) is rare disease in neonates, characterized by hypercalcemia, failure to thrive, skeletal demineralization and often multiple fractures. NSPHT induced hypercalcemia is often refractory to conventional medical therapy and may demand technically challenging surgery. We herein report a case of a neonate with NSPHT, due to novel mutation, who failed medical therapy including calcimimetics and underwent total parathyroidectomy with tracheostomy in our setup.

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