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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

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