1 The Department of Pediatrics, University of North Carolina, Chapel Hill
The case of a premature infant with the onset of hypercalcemia and apparent primary hyperparathyroidism in the immediate neonatal period is presented. Although the treatment in most such cases has been parathyroidectomy, this infant was managed medically and survived infancy without apparent complications. We believe her disorder represents the neonatal manifestations of familial hypocalciuric hypercalcemia. Her course supports the contention that this disorder may be self-limited in some infants and that appropriate medical management can preclude the need for surgical intervention in selected cases.
Key Words: hyperparathyroidism hypercalcemia hypocalciuria osteopenia newborn
Submitted on August 11, 1987
Accepted on December 11, 1987
This article has been cited by other articles:
![]() |
L. Fox, J. Sadowsky, K. P. Pringle, A. Kidd, J. Murdoch, D. E.C. Cole, and E. Wiltshire Neonatal Hyperparathyroidism and Pamidronate Therapy in an Extremely Premature Infant Pediatrics, November 1, 2007; 120(5): e1350 - e1354. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Zajickova, J. Vrbikova, L. Canaff, P. D. Pawelek, D. Goltzman, and G. N. Hendy Identification and Functional Characterization of a Novel Mutation in the Calcium-Sensing Receptor Gene in Familial Hypocalciuric Hypercalcemia: Modulation of Clinical Severity by Vitamin D Status J. Clin. Endocrinol. Metab., July 1, 2007; 92(7): 2616 - 2623. [Abstract] [Full Text] [PDF] |
||||