1. Activating calcium-sensing receptor gene variants in children: a case study of infant hypocalcaemia and literature review.
- Author
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Thim SB, Birkebaek NH, Nissen PH, and Høst C
- Subjects
- Calcium therapeutic use, Female, Genetic Variation, Humans, Hypercalciuria diagnosis, Hypercalciuria drug therapy, Hypocalcemia diagnosis, Hypocalcemia drug therapy, Hypoparathyroidism diagnosis, Hypoparathyroidism drug therapy, Hypoparathyroidism genetics, Infant, Hypercalciuria genetics, Hypocalcemia genetics, Hypoparathyroidism congenital, Receptors, Calcium-Sensing genetics, Receptors, Calcium-Sensing physiology
- Abstract
Unlabelled: Autosomal dominant hypocalcaemia (ADH) is caused by activating variants in the calcium-sensing receptor (CASR) gene, but detailed information on the paediatric phenotype is limited. The current paper presents a case of severe ADH and systematically reviews the literature on ADH in children., Conclusion: We found that the severity of clinical neurological symptoms was inversely related to serum calcium levels and a high prevalence of renal calcifications and/or basal ganglia calcifications in children with ADH., (©2014 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.)
- Published
- 2014
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