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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Detalles Bibliográficos
Autores principales: Wang, Feifei, Hu, Jia, Mei, Chao, Lin, Xia, Zhang, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458196/
https://www.ncbi.nlm.nih.gov/pubmed/32871939
http://dx.doi.org/10.1097/MD.0000000000021940

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458196/
https://www.ncbi.nlm.nih.gov/pubmed/32871939
http://dx.doi.org/10.1097/MD.0000000000021940

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