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Osteomalacia with low alkaline phosphatase: a not so rare condition with important consequences
Hypophosphatasia is a genetic disorder, characterised by a dysfunctional tissue-non-specific isoenzyme of alkaline phosphatase that impacts bone metabolism and predisposes to osteomalacia or rickets. The clinical presentation is very diverse, depending on the age of onset and the severity of the dis...
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| Foilsithe in: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Publishing Group
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4735159/ https://ncbi.nlm.nih.gov/pubmed/26823351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-212827 |
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