Case of hypomagnesemia with secondary hypocalcemia with a novel TRPM6 mutation

Neurol India. 2018 Nov-Dec;66(6):1795-1800. doi: 10.4103/0028-3886.246240.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Review

MeSH terms

  • Genetic Predisposition to Disease*
  • Humans
  • Hypocalcemia / diagnosis
  • Hypocalcemia / genetics*
  • Infant
  • Magnesium
  • Magnesium Deficiency / congenital*
  • Magnesium Deficiency / diagnosis
  • Magnesium Deficiency / genetics
  • Male
  • Mutation / genetics*
  • TRPM Cation Channels / genetics*

Substances

  • TRPM Cation Channels
  • TRPM6 protein, human
  • Magnesium

Supplementary concepts

  • Hypomagnesemia 1, Intestinal