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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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Príomhchruthaitheoirí: Giada Bennati (Údar), Mario Cirino (Údar), Giulia Benericetti (Údar), Natalia Maximova (Údar), Monica Zanier (Údar), Federico Pigato (Údar), Anna Parzianello (Údar), Alessandra Maestro (Údar), Egidio Barbi (Údar), Davide Zanon (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: MDPI AG, 2023-05-01T00:00:00Z.
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