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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550883/ http://dx.doi.org/10.1210/js.2019-MON-540 |