Familial Hypomagnesemia With Secondary Hypocalcemia: A Case Report

Familial hypomagnesemia with secondary hypocalcemia is a rare genetic disorder of magnesium metabolism that presents with refractory seizures during infancy. It is caused by loss-of-function mutations in the gene encoding transient receptor potential cation channel member 6 (TRPM6). Herein we report...

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Detalles Bibliográficos
Autores principales: Gazzaz, Nour, Alghamdi, Maha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702611/
https://www.ncbi.nlm.nih.gov/pubmed/34963857
http://dx.doi.org/10.7759/cureus.19847

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702611/
https://www.ncbi.nlm.nih.gov/pubmed/34963857
http://dx.doi.org/10.7759/cureus.19847

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