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Hypophosphatemic Rickets in Siblings: A Rare Case Report
Hypophosphatemic rickets (HR) is a type of hereditary rickets characterized by persistent hypophosphatemia and hyperphosphaturia. The most predominant type is inherited in an X-linked fashion and caused by mutation in the gene encoding the phosphate-regulating endopeptidase homolog, X-linked (PHEX),...
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| 出版年: | Case Rep Dent |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi Publishing Corporation
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4906197/ https://ncbi.nlm.nih.gov/pubmed/27340574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/4803167 |
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