Juvenile Paget’s Disease In An Iranian Kindred With Vitamin D Deficiency And Novel Homozygous TNFRSF11B Mutation

Juvenile Paget’s disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline phosphatase (ALP) activity emanating from generalized acceleration of skeletal turnover. Affected infants and children typically suffer bone pain and fractures and deformiti...

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Hlavní autoři: Saki, Forough, Karamizadeh, Zohreh, Nasirabadi, Shiva, Mumm, Steven, McAlister, William H., Whyte, Michael P.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2013
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3663917/
https://ncbi.nlm.nih.gov/pubmed/23322328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.1868
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