Literature DB >> 17899212

Report of a family with two different hereditary diseases leading to early nephrocalcinosis.

Rosa Vargas-Poussou1, Pierre Cochat, Nelly Le Pottier, Isabelle Roncelin, Aurelia Liutkus, Anne Blanchard, Xavier Jeunemaître.   

Abstract

The etiologies of early onset nephrocalcinosis in consanguineous families include five major inherited recessive disorders: primary hyperoxaluria (PH), familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), distal renal tubular acidosis (dRTA), hereditary hypophosphatemic rickets with hypercalciuria (HHRH) and antenatal Bartter syndrome. In this paper, we describe two girls from consanguineous parents with early onset nephrocalcinosis. Based on both clinical and biochemical assessment in combination with molecular genetics, we have shown that the etiology of nephrocalcinosis is different in each girl: one had FHHNC and her sister had dRTA.

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Year:  2007        PMID: 17899212     DOI: 10.1007/s00467-007-0584-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  15 in total

Review 1.  Renal tubular acidosis: the clinical entity.

Authors:  Juan Rodríguez Soriano
Journal:  J Am Soc Nephrol       Date:  2002-08       Impact factor: 10.121

Review 2.  An unusual patient with hypercalciuria, recurrent nephrolithiasis, hypomagnesemia and G227R mutation of Paracellin-1. An unusual patient with hypercalciuria and hypomagnesemia unresponsive to thiazide diuretics.

Authors:  Faruk Kutluturk; Berna Temel; Bora Uslu; Ferihan Aral; Adil Azezli; Yusuf Orhan; Martin Konrad; Nese Ozbey
Journal:  Horm Res       Date:  2006-06-27

Review 3.  Hypomagnesaemia-hypercalciuria-nephrocalcinosis: a report of nine cases and a review.

Authors:  V Benigno; C S Canonica; A Bettinelli; R O von Vigier; A C Truttmann; M G Bianchetti
Journal:  Nephrol Dial Transplant       Date:  2000-05       Impact factor: 5.992

4.  Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.

Authors:  Martin Konrad; Andre Schaller; Dominik Seelow; Amit V Pandey; Siegfried Waldegger; Annegret Lesslauer; Helga Vitzthum; Yoshiro Suzuki; John M Luk; Christian Becker; Karl P Schlingmann; Marcel Schmid; Juan Rodriguez-Soriano; Gema Ariceta; Francisco Cano; Ricardo Enriquez; Harald Juppner; Sevcan A Bakkaloglu; Matthias A Hediger; Sabina Gallati; Stephan C F Neuhauss; Peter Nurnberg; Stefanie Weber
Journal:  Am J Hum Genet       Date:  2006-09-19       Impact factor: 11.025

5.  Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.

Authors:  Bettina Lorenz-Depiereux; Anna Benet-Pages; Gertrud Eckstein; Yardena Tenenbaum-Rakover; Janine Wagenstaller; Dov Tiosano; Ruth Gershoni-Baruch; Norbert Albers; Peter Lichtner; Dirk Schnabel; Ze'ev Hochberg; Tim M Strom
Journal:  Am J Hum Genet       Date:  2005-12-09       Impact factor: 11.025

6.  Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle.

Authors:  A Blanchard; X Jeunemaitre; P Coudol; M Dechaux; M Froissart; A May; R Demontis; A Fournier; M Paillard; P Houillier
Journal:  Kidney Int       Date:  2001-06       Impact factor: 10.612

7.  Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

Authors:  Rosa Vargas-Poussou; Pascal Houillier; Nelly Le Pottier; Laurence Strompf; Chantal Loirat; Véronique Baudouin; Marie-Alice Macher; Michèle Déchaux; Tim Ulinski; François Nobili; Philippe Eckart; Robert Novo; Mathilde Cailliez; Rémi Salomon; Hubert Nivet; Pierre Cochat; Ivan Tack; Anne Fargeot; François Bouissou; Gwenaelle Roussey Kesler; Stéphanie Lorotte; Nathalie Godefroid; Valérie Layet; Gilles Morin; Xavier Jeunemaître; Anne Blanchard
Journal:  J Am Soc Nephrol       Date:  2006-04-12       Impact factor: 10.121

8.  Pathophysiology of the renal acidification defect present in the syndrome of familial hypomagnesaemia-hypercalciuria.

Authors:  J Rodríguez-Soriano; A Vallo
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

Review 9.  Bartter syndrome.

Authors:  Steven C Hebert
Journal:  Curr Opin Nephrol Hypertens       Date:  2003-09       Impact factor: 2.894

10.  Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.

Authors:  Matthias T F Wolf; Jörg Dötsch; Martin Konrad; Michael Böswald; Wolfgang Rascher
Journal:  Pediatr Nephrol       Date:  2002-06-11       Impact factor: 3.714

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  8 in total

1.  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.

Authors:  Astrid Godron; Jérôme Harambat; Valérie Boccio; Anne Mensire; Adrien May; Claire Rigothier; Lionel Couzi; Benoit Barrou; Michel Godin; Dominique Chauveau; Stanislas Faguer; Marion Vallet; Pierre Cochat; Philippe Eckart; Geneviève Guest; Vincent Guigonis; Pascal Houillier; Anne Blanchard; Xavier Jeunemaitre; Rosa Vargas-Poussou
Journal:  Clin J Am Soc Nephrol       Date:  2012-03-15       Impact factor: 8.237

2.  Why is hypercalciuria absent at diagnosis in some children with ATP6V1B1 mutation?

Authors:  Hsin-Yun Tsai; Shih-Hua Lin; Chun-Chen Lin; Fu-Yuan Huang; Ming-Dar Lee; Jeng-Daw Tsai
Journal:  Pediatr Nephrol       Date:  2011-05-26       Impact factor: 3.714

3.  Growth hormone therapy in HHRH.

Authors:  Guido Filler; Clara Schott; Fabio Rosario Salerno; Andrea Ens; Christopher William McIntyre; Maria Esther Díaz González de Ferris; Robert Stein
Journal:  Bone Rep       Date:  2022-05-18

Review 4.  Acidosis and Urinary Calcium Excretion: Insights from Genetic Disorders.

Authors:  R Todd Alexander; Emmanuelle Cordat; Régine Chambrey; Henrik Dimke; Dominique Eladari
Journal:  J Am Soc Nephrol       Date:  2016-07-28       Impact factor: 10.121

5.  Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations.

Authors:  Majdi Nagara; Konstantinos Voskarides; Sonia Nouira; Nizar Ben Halim; Rym Kefi; Hajer Aloulou; Lilia Romdhane; Rim Ben Abdallah; Faten Ben Rhouma; Khaoula Aissa; Lamia Boughamoura; Thouraya Kammoun; Hatem Azzouz; Saoussen Abroug; Hathemi Ben Turkia; Abdelkarim Ayadi; Ridha Mrad; Imen Chabchoub; Mongia Hachicha; Jalel Chemli; Constantinos Deltas; Sonia Abdelhak
Journal:  Genet Test Mol Biomarkers       Date:  2014-10-06

6.  SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuria.

Authors:  Shirin Hasani-Ranjbar; Mahsa M Amoli; Azadeh Ebrahim-Habibi; Ehsan Dehghan; Akbar Soltani; Parvin Amiri; Bagher Larijani
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-06

7.  An expanded syndrome of dRTA with hearing loss, hyperoxaluria and beta2-microglobulinuria.

Authors:  Lawrence Copelovitch; Bernard S Kaplan
Journal:  NDT Plus       Date:  2010-07-12

Review 8.  Claudins in Renal Physiology and Pathology.

Authors:  Caroline Prot-Bertoye; Pascal Houillier
Journal:  Genes (Basel)       Date:  2020-03-10       Impact factor: 4.096

  8 in total

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