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

• Main Authors: Hüsniye Yücel (Author), Çiğdem Genç Sel (Author), Çiğdem Seher Kasapkara (Author), Gülin Karacan Küçükali (Author), Senay Savas-Erdeve (Author), Ülkühan Öztoprak (Author), Serdar Ceylaner (Author), Saliha Şenel (Author), Meltem Akçaboy (Author)
• Format: Book
• Published: Galenos Yayincilik, 2021-03-01T00:00:00Z.
• Subjects: article
• Online Access: 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...