Familial hypomagnesemia with secondary hypocalcemia mimicking neurodegenerative disorder

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作者：Mahesh Kamate ; Neha Singh ; Supriya Patil
关键词：Calcium ; Developmental delay ; Drug ; resistant seizures ; Magnesium
刊名：Indian Pediatrics
出版年：2015
出版时间：June 2015
年：2015
卷：52
期：6
页码：521-522
全文大小：368 KB
参考文献：1.Assadi F. Hypomagnesemia: An evidence-based approach to clinical cases. Iranian J Kidney Dis. 2010;4:13鈥?.
2.Joshi R, Phatarpekar A. Hypomagnesaemia with secondary hypocalcaemia due to TRPM6 gene mutation. Sri Lanka J Child Health. 2012;41:205鈥?6.
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鈥?7.View Article
4.Konrad M, Weber S. Recent advances in molecular genetics of hereditary magnesium-losing disorders. J Am Soc Nephrol. 2003;14:249鈥?0.PubMed View Article
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鈥?4.PubMed View Article
作者单位：Mahesh Kamate (1)
Neha Singh (1)
Supriya Patil (1)

1. Professor of Pediatrics, KLE University鈥檚 J N Medical College, Belgaum, 590 010, Karnataka, India
刊物主题：Pediatrics; Pediatric Surgery; Maternal and Child Health;
出版者：Springer India
ISSN：0974-7559

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