Literature DB >> 3298795

Renal magnesium wasting in two families with autosomal dominant inheritance.

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.

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Year:  1987        PMID: 3298795     DOI: 10.1038/ki.1987.120

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  8 in total

Review 1.  The long-term complications of the inherited tubulopathies: an adult perspective.

Authors:  Maryam Khosravi; Stephen B Walsh
Journal:  Pediatr Nephrol       Date:  2014-02-25       Impact factor: 3.714

Review 2.  Genetics of hereditary disorders of magnesium homeostasis.

Authors:  Karl P Schlingmann; Martin Konrad; Hannsjörg W Seyberth
Journal:  Pediatr Nephrol       Date:  2003-11-22       Impact factor: 3.714

Review 3.  Hypomagnesaemia of hereditary renal origin.

Authors:  J Rodríguez-Soriano; A Vallo; M García-Fuentes
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

4.  Hereditary isolated renal magnesium loss maps to chromosome 11q23.

Authors:  I C Meij; K Saar; L P van den Heuvel; G Nuernberg; M Vollmer; F Hildebrandt; A Reis; L A Monnens; N V Knoers
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

5.  Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.

Authors:  Daan Viering; Karl P Schlingmann; Marguerite Hureaux; Tom Nijenhuis; Andrew Mallett; Melanie M Y Chan; André van Beek; Albertien M van Eerde; Jean-Marie Coulibaly; Marion Vallet; Stéphane Decramer; Solenne Pelletier; Günter Klaus; Martin Kömhoff; Rolf Beetz; Chirag Patel; Mohan Shenoy; Eric J Steenbergen; Glenn Anderson; Ernie M H F Bongers; Carsten Bergmann; Daan Panneman; Richard J Rodenburg; Robert Kleta; Pascal Houillier; Martin Konrad; Rosa Vargas-Poussou; Nine V A M Knoers; Detlef Bockenhauer; Jeroen H F de Baaij
Journal:  J Am Soc Nephrol       Date:  2021-10-04       Impact factor: 10.121

6.  Quadriparesis in diabetes due to dyselectrolytemia.

Authors:  Arundhati Dasgupta; Uma K Saikia; Dipti Sharma; Mihir Saikia; S Dutta Choudhury
Journal:  Indian J Endocrinol Metab       Date:  2010-01

Review 7.  The genetic spectrum of Gitelman(-like) syndromes.

Authors:  Karl P Schlingmann; Jeroen H F de Baaij
Journal:  Curr Opin Nephrol Hypertens       Date:  2022-07-11       Impact factor: 3.416

Review 8.  Inherited forms of renal hypomagnesemia: an update.

Authors:  Nine V A M Knoers
Journal:  Pediatr Nephrol       Date:  2008-09-26       Impact factor: 3.651

  8 in total

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