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A Rare Case of Hypophosphataemic Osteomalacia in von Recklinghausen Neurofibromatosis
BACKGROUND: Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is a one of the more common hereditary autosomal disorders. However, osteomalacia in neurofibromatosis type 1 is very rare tumour-induced osteomalacia; fibroblast growth factor-23 is usually implicated. PATIENTS AN...
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| Pubblicato in: | Eur J Case Rep Intern Med |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SMC Media Srl
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8191358/ https://ncbi.nlm.nih.gov/pubmed/34123954 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12890/2021_002618 |
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