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Case report: rare skeletal manifestations in a child with primary hyperparathyroidism
BACKGROUND: Primary hyperparathyroidism (PHPT) is uncommon among children with an incidence of 1:300,000. This diagnosis is often missed in children in contrast to adults where it is detected at a pre symptomatic stage due to routine blood investigations. Etiology of PHPT can be due to adenoma, hype...
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| Yayımlandı: | BMC Endocr Disord |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5521059/ https://ncbi.nlm.nih.gov/pubmed/28732535 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12902-017-0197-z |
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