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A novel CaSR mutation presenting as a severe case of neonatal familial hypocalciuric hypercalcemia
BACKGROUND: Familial Hypocalciuric Hypercalcemia (FHH) is a generally benign disorder caused by heterozygous inactivating mutations in the Calcium-Sensing Receptor (CaSR) gene resulting in altered calcium metabolism. OBJECTIVE: We report a case of unusually severe neonatal FHH due to a novel CaSR ge...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3465174/ https://ncbi.nlm.nih.gov/pubmed/22620673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1687-9856-2012-13 |
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