Compounded Effervescent Magnesium for Familial Hypomagnesemia: A Case Report

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disorder affecting <1/1,000,000 people. It is caused by mutations in the CLDN16 (FHHNC Type 1) or CLDN19 (FHHNC Type 2) genes, which are located on Chromosomes 3q27 and 1p34.2, respectively. The...

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Detalles Bibliográficos
Autores principales: Bennati, Giada, Cirino, Mario, Benericetti, Giulia, Maximova, Natalia, Zanier, Monica, Pigato, Federico, Parzianello, Anna, Maestro, Alessandra, Barbi, Egidio, Zanon, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305453/
https://www.ncbi.nlm.nih.gov/pubmed/37375733
http://dx.doi.org/10.3390/ph16060785

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305453/
https://www.ncbi.nlm.nih.gov/pubmed/37375733
http://dx.doi.org/10.3390/ph16060785

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