Familial hypomagnesemia with secondary hypocalcemia mimicking neurodegenerative disorder
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s13312-015-0668-0.pdf
Reference5 articles.
1. Assadi F. Hypomagnesemia: An evidence-based approach to clinical cases. Iranian J Kidney Dis. 2010;4:13–7.
2. Joshi R, Phatarpekar A. Hypomagnesaemia with secondary hypocalcaemia due to TRPM6 gene mutation. Sri Lanka J Child Health. 2012;41:205–06.
3. Chubanov V, Schlingmann K, Waring J, Heinzinger J, Kaske S, Waldegger S, et al. Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6. J Biolog Chem. 2007;282:7656–67.
4. Konrad M, Weber S. Recent advances in molecular genetics of hereditary magnesium-losing disorders. J Am Soc Nephrol. 2003;14:249–60.
5. Al-Shibli A, Konrad M, Altay W, Masri O, Al-Gazali L, Attrach I. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): Report of three cases with a novel mutation in CLDN19 Gene. Saudi J Kidney Dis Transpl. 2013;24:338–44.
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1. A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant;Indian Pediatrics Case Reports;2024-07
2. Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature;CEN Case Reports;2023-03-26
3. Familial Hypomagnesemia with Secondary Hypocalcemia Presenting as Refractory Seizures;Annals of Indian Academy of Neurology;2023
4. Familial hypomagnesemia with hypocalcemia: a rare cause of infantile seizures;CEN Case Reports;2022-09-21
5. Familial Hypomagnesemia With Secondary Hypocalcemia: A Case Report;Cureus;2021-11-23
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