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

• मुख्य लेखकों: Hüsniye Yücel (लेखक), Çiğdem Genç Sel (लेखक), Çiğdem Seher Kasapkara (लेखक), Gülin Karacan Küçükali (लेखक), Senay Savas-Erdeve (लेखक), Ülkühan Öztoprak (लेखक), Serdar Ceylaner (लेखक), Saliha Şenel (लेखक), Meltem Akçaboy (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Galenos Yayincilik, 2021-03-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...