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De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidismopen access
- Authors
- Moon, J.-E.[Moon, J.-E.]; Lee, S.-J.[Lee, S.-J.]; Parkm, S.-H.[Parkm, S.-H.]; Kim, J.[Kim, J.]; Jin, D.-K.[Jin, D.-K.]; Ko, C.W.[Ko, C.W.]
- Issue Date
- Jun-2018
- Publisher
- Korean society of pediatric endocrinology
- Keywords
- Calcium-sensing receptors; Hypercalciuric hypocalcemia; Hypoparathyroidism; Mutation
- Citation
- Annals of Pediatric Endocrinology and Metabolism, v.23, no.2, pp.107 - 111
- Indexed
- SCOPUS
- Journal Title
- Annals of Pediatric Endocrinology and Metabolism
- Volume
- 23
- Number
- 2
- Start Page
- 107
- End Page
- 111
- ISSN
- 2287-1012
- Abstract
- Autosomal-dominant hypocalcemia with hypercalciuria (ADHH) is a genetic disease characterized by hypoparathyroidism with hypercalciuria. Most patients with ADHH have calcium-sensing receptor (CaSR) gene mutations. The CaSR gene controls parathyroid secretions, and mutations in this gene can be detected via changes in serum calcium level. The activating mutation of the CaSR gene results in familial or sporadic ADHH. Most activating mutations of the CaSR gene are reportedly de novo missense mutations. This is the first case report of a novel activating variant of the CaSR gene in a neonate with congenital hypoparathyroidism with hypomagnesemia and hypercalciuria. We also report the 3-month follow-up management of the patient. © 2018 Annals of Pediatric Endocrinology & Metabolism.
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Collections - Medicine > Department of Medicine > 1. Journal Articles
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