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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yücel, Hüsniye, Genç Sel, Çiğdem, Kasapkara, Çiğdem Seher, Karacan Küçükali, Gülin, Savas-Erdeve, Senay, Öztoprak, Ülkühan, Ceylaner, Serdar, Şenel, Saliha, Akçaboy, Meltem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947728/
https://www.ncbi.nlm.nih.gov/pubmed/32302086
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947728/
https://www.ncbi.nlm.nih.gov/pubmed/32302086
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0004

Ejemplares similares