Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Sign Up to like & getrecommendations! Published in 2019 at "Gene"
DOI: 10.1016/j.gene.2018.12.024
Abstract: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an autosomal-recessive renal tubular disorder characterized by excessive urinary losses of magnesium and calcium, bilateral nephrocalcinosis and progressive chronic renal failure in childhood or adolescence. The disease is… read more here.
Keywords: mutation; nephrocalcinosis; hypomagnesemia hypercalciuria; hypercalciuria nephrocalcinosis ... See more keywords
Compounded Effervescent Magnesium for Familial Hypomagnesemia: A Case Report
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DOI: 10.3390/ph16060785
Abstract: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disorder affecting read more here.
Keywords: magnesium; familial hypomagnesemia; report; case ... See more keywords