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Renal magnesium wasting in two families with autosomal dominant inheritance
Authors:W B Geven  L A Monnens  H L Willems  W C Buijs  B G ter Haar
Abstract:
Hypomagnesemia due to isolated renal magnesium loss was demonstrated in two unrelated families with autosomal dominant mode of inheritance. Magnesium infusions performed in two patients showed not only a reduced renal magnesium threshold but also a lowered renal tubular maximum for magnesium. All members of both families who presented with hypomagnesemia had also a lowered excretion of calcium in the urine, presumably as a consequence of increased reabsorption in Henle's loop.
Keywords:
引证文献(本文共被引3次):
[1]、Nine V. A. M. Knoers.Inherited forms of renal hypomagnesemia: an update[J].Pediatric Nephrology,2009,24(4):697-705.
[2]、Iwan C Meij,Lambert P W J van den Heuvel,Sies Hemmes,Walter A van der Vliet,Johannes L Willems,Leo A H Monnens,Nine V A M Knoers.Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss.[J].Nephrology Dialysis Transplantation,2003,18(3):512-516.
[3]、B Bastani,G Pandurangan.Intraperitoneal route of magnesium sulphate supplementation in a patient with severe renal magnesium wasting.[J].Nephrology Dialysis Transplantation,2001,16(10):2086-2089.
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