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Familial hypocalciuric hypercalcemia with a de novo heterozygous mutation of calcium-sensing receptor
A de novo heterozygous inactivating mutation of calcium-sensing receptor (CASR) gene typically causes neonatal hyperparathyroidism (NHPT) with moderate hypercalcemia and hyperparathyroid bone disease. We present a case of asymptomatic hypocalciuric hypercalcemia with a de novo heterozygous mutation...
Autores principales: | Taki, Katsumi, Kogai, Takahiko, Sakumoto, Junko, Namatame, Takashi, Hishinuma, Akira |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439728/ https://www.ncbi.nlm.nih.gov/pubmed/26019872 http://dx.doi.org/10.1530/EDM-15-0016 |
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