Document Type

Article

Publication Date

5-1-2013

Identifier

DOI: 10.1002/jbmr.1838

Abstract

Secondary hyperparathyroidism from inadequate calcium absorption in the gut, is the underlying pathophysiology for rachitic changes in hereditary vitamin D-resistant rickets (HVDRR). We describe a novel use of Cinacalcet to treat a child with HVDRR in whom conventional modes of therapy had to be discontinued. Cinacalcet therapy with high-dose oral calcium effectively normalized the metabolic abnormalities and bone condition. The relative ease of administration of the calcimimetic as a once- or twice-daily oral preparation, compared with traditional intravenous calcium administration, should encourage its move to the frontline of treatment of the disorder.

Journal Title

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Volume

28

Issue

5

First Page

992

Last Page

996

MeSH Keywords

Cinacalcet; Familial Hypophosphatemic Rickets; Humans; Infant; Male; Naphthalenes; Treatment Outcome

Share

COinS