Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

Hypomagnesemia is a rare cause of seizures in childhood but should be kept in mind in recurrent and intractable seizures and hypocalcemia in communities where consanguineous marriages are common. Familial hypomagnesemia with secondary hypocalcemia is a rare genetic cause of hypomagnesemia, due to va...

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Xehetasun bibliografikoak

Egile Nagusiak:	Hüsniye Yücel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas-Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akçaboy
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Pediatric Endocrinology and Diabetes Society 2021-03-01
Saila:	JCRPE
Gaiak:	hypocalcemia hypomagnesemia trpm6 transient receptor potential melastatin 6
Sarrera elektronikoa:	http://www.jcrpe.org/archives/archive-detail/article-preview/treatment-difficulties-in-hypomagnesemia-secondary/37305
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