A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory

Heterozygous inactivating mutations in the calcium-sensing receptor (CaSR) gene are known to cause familial hypocalciuric hypercalcemia (FHH), usually a benign form of hypercalcemia without symptoms of a disrupted calcium homeostasis. FHH can be mistaken for the more common primary hyperparathyroidi...

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Detalles Bibliográficos
Autores principales: Carlsson, Elin Rebecka, Toft Nielsen, Mai-Britt, Høgh, Anne Mette, Veggerby Grønlund, Rikke, Fenger, Mogens, Ambye, Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393866/
https://www.ncbi.nlm.nih.gov/pubmed/30895164
http://dx.doi.org/10.1155/2019/9468252

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393866/
https://www.ncbi.nlm.nih.gov/pubmed/30895164
http://dx.doi.org/10.1155/2019/9468252

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