Abstract
Vitamin D-dependent rickets type 1 VDDR-1 is a recessive inherited disorder with impaired activation of vitamin D, caused by mutations in CYP27B1. We present long-time follow-up of a case with a novel mutation including high-resolution peripheral quantitative computed tomography of the bone. Adequate treatment resulted in a normalized phenotype.
Originalsprog | Engelsk |
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Tidsskrift | Clinical Case Reports |
Vol/bind | 3 |
Udgave nummer | 12 |
Sider (fra-til) | 1012-1016 |
ISSN | 2050-0904 |
DOI | |
Status | Udgivet - dec. 2015 |