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MON-540 Familial Hypocalciuric Hypercalcemia Diagnosed in a 63-Year-Old Female
Background Familial Hypocalciuric Hypercalcemia (FHH) is a rare autosomal dominant genetic disorder which causes impaired calcium sensing receptor (CaSR) function which is located in the parathyroid and kidneys. This disorder leads to hypercalcemia, hypocalciuria and normal to moderately elevated pa...
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| Yayımlandı: | J Endocr Soc |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Endocrine Society
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6550883/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-540 |
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