Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/28029
Title: Severe hypercalcemia in a 9-year-old Brazilian girl due to a novel inactivating mutation of the calcium-sensing receptor
Authors: Miyashiro, Kozue [UNIFESP]
Kunii, Ilda Shizue [UNIFESP]
Della Manna, Thais
Menezes, Hamilton C. de
Damiani, Durval
Setian, Nuvarte
Hauache, Omar Magid [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Issue Date: 1-Dec-2004
Publisher: Endocrine Soc
Citation: Journal of Clinical Endocrinology & Metabolism. Chevy Chase: Endocrine Soc, v. 89, n. 12, p. 5936-5941, 2004.
Abstract: Familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) are consequent to inactivating mutations of the calcium-sensing receptor (CaR) gene. FHH is usually associated with heterozygous inactivating mutations of the CaR gene, whereas NSHPT is usually due to homozygous inactivation of the CaR gene. FHH is generally asymptomatic and is characterized by mild to moderate lifelong hypercalcemia, relative hypocalciuria, and normal intact PTH, whereas individuals with NSHPT frequently show life-threatening hypercalcemia. in this study, we report a novel inactivating mutation of the CaR gene, identified in a 9-yr-old Brazilian girl who was found to be severely hypercalcemic during investigation of a 6-month history of headaches and vomits. Direct sequencing of the CaR gene from this patient showed a novel homozygous mutation (L13P) in exon 2. Functional characterization by intracellular calcium measurement by fluorometry showed that the mutant receptor had a dose-response curve shifted to the right relative to that of wild type. the proband's consanguineous parents, who had mild asymptomatic hypercalcemia, showed the same mutation in the heterozygous form. the mutation described in this study is the inactivating missense mutation present at the most N-terminal end among the known CaR missense mutations. This study reinforces the fact that patients with homozygous inactivation of the CaR gene may present with severe hypercalcemia in different phases of life.
URI: http://repositorio.unifesp.br/handle/11600/28029
ISSN: 0021-972X
Other Identifiers: http://dx.doi.org/10.1210/jc.2004-1046
Appears in Collections:Em verificação - Geral

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