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Familial hypocalciuric hypercalcemia caused by homozygous CaSR gene mutation: A case report of a family
INTRODUCTION: Familial hypocalciuric hypercalcemia (FHH) is a group of autosomal dominant genetic diseases with persistent hypercalcemia and hypocalciuria. The calcium-sensitive receptor (CaSR) plays an important role in calcium and phosphorus metabolism. PATIENT CONCERNS: A 32-year-old man who had...
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| Publicado en: | Medicine (Baltimore) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Lippincott Williams & Wilkins
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7458196/ https://ncbi.nlm.nih.gov/pubmed/32871939 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000021940 |
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