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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Bibliographic Details
Main Authors:	Tonyushkina, Ksenia N, O’Connor, Stephen, Dunbar, Nancy S
Format:	Artigo
Language:	Inglês
Published:	BioMed Central 2012
Subjects:	Case Report
Online Access:	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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A novel CaSR mutation presenting as a severe case of neonatal familial hypocalciuric hypercalcemia

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