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Xu, C. Hypomagnesemia with Secondary Hypocalcemia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4256 (accessed on 29 September 2026).
Xu C. Hypomagnesemia with Secondary Hypocalcemia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4256. Accessed September 29, 2026.
Xu, Camila. "Hypomagnesemia with Secondary Hypocalcemia" Encyclopedia, https://encyclopedia.pub/entry/4256 (accessed September 29, 2026).
Xu, C. (2020, December 23). Hypomagnesemia with Secondary Hypocalcemia. In Encyclopedia. https://encyclopedia.pub/entry/4256
Xu, Camila. "Hypomagnesemia with Secondary Hypocalcemia." Encyclopedia. Web. 23 December, 2020.
Hypomagnesemia with Secondary Hypocalcemia
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Hypomagnesemia with secondary hypocalcemia is an inherited condition caused by the body's inability to absorb and retain magnesium that is taken in through the diet. As a result, magnesium levels in the blood are severely low (hypomagnesemia).

genetic conditions

References

  1. Chubanov V, Gudermann T, Schlingmann KP. Essential role for TRPM6 inepithelial magnesium transport and body magnesium homeostasis. Pflugers Arch.2005 Oct;451(1):228-34.
  2. Katayama K, Povalko N, Yatsuga S, Nishioka J, Kakuma T, Matsuishi T, Koga Y.New TRPM6 mutation and management of hypomagnesaemia with secondaryhypocalcaemia. Brain Dev. 2015 Mar;37(3):292-8. doi:10.1016/j.braindev.2014.06.006.
  3. Lainez S, Schlingmann KP, van der Wijst J, Dworniczak B, van Zeeland F, KonradM, Bindels RJ, Hoenderop JG. New TRPM6 missense mutations linked tohypomagnesemia with secondary hypocalcemia. Eur J Hum Genet. 2014Apr;22(4):497-504. doi: 10.1038/ejhg.2013.178.
  4. Schlingmann KP, Sassen MC, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D,Syrrou M, Prebble JJ, Cole DE, Metzger DL, Rahman S, Tajima T, Shu SG, Waldegger S, Seyberth HW, Konrad M. Novel TRPM6 mutations in 21 families with primaryhypomagnesemia and secondary hypocalcemia. J Am Soc Nephrol. 2005Oct;16(10):3061-9.
  5. Schlingmann KP, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K,Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth HW, Konrad M. Hypomagnesemia with secondary hypocalcemia is caused bymutations in TRPM6, a new member of the TRPM gene family. Nat Genet. 2002Jun;31(2):166-70.
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Update Date: 23 Dec 2020
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