PTH(1-34) Replacement Therapy in a Child With Hypoparathyroidism Caused by a Sporadic Calcium Receptor Mutation

Autosomal dominant hypocalcemia (ADH) is an inherited form of hypoparathyroidism caused by activating mutations in the calcium-sensing receptor (CaR). Treatment with PTH(1-34) may be superior to conventional therapy but is contraindicated in children, and long-term effects on the skeleton are unknow...

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Detalhes bibliográficos
Main Authors: Theman, Todd A, Collins, Michael T, Dempster, David W, Zhou, Hua, Reynolds, James C, Brahim, Jaime S, Roschger, Paul, Klaushofer, Klaus, Winer, Karen K.
Formato: Artigo
Idioma:Inglês
Publicado em: Amer Soc Bone & Mineral Res. 2009
Assuntos:
Clinical Vignette
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2672210/
https://ncbi.nlm.nih.gov/pubmed/19063686
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1359/JBMR.081233
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