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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...
Autores principales: | Carlsson, Elin Rebecka, Toft Nielsen, Mai-Britt, Høgh, Anne Mette, Veggerby Grønlund, Rikke, Fenger, Mogens, Ambye, Louise |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
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 |
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