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

• প্রধান লেখক: Hüsniye Yücel (লেখক), Çiğdem Genç Sel (লেখক), Çiğdem Seher Kasapkara (লেখক), Gülin Karacan Küçükali (লেখক), Senay Savas-Erdeve (লেখক), Ülkühan Öztoprak (লেখক), Serdar Ceylaner (লেখক), Saliha Şenel (লেখক), Meltem Akçaboy (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Galenos Yayincilik, 2021-03-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

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...