Literature DB >> 21633858

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentations.

Hilary H Seeley1, Lindsey A Loomba-Albrecht, Mato Nagel, Lavjay Butani, Andrew A Bremer.   

Abstract

BACKGROUND: This article summarizes the varying clinical manifestations of three siblings with familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) caused by the same genetic lesion.
METHODS: The medical records of three siblings with FHHNC (one girl and two boys, aged 6 to 12 years) were reviewed and the clinical manifestations and treatment of their disease were described.
RESULTS: Despite varying phenotypes, each sibling had the same genetic lesion-a novel homozygous mutation in CLDN16 (c.211A>G, M71V).
CONCLUSION: Although FHHNC is a rare disorder, this report is significant for the following reasons: (i) it describes a novel CLDN16 mutation causing FHHNC, adding to the literature of FHHNC-causing CLDN16 mutations; (ii) it suggests that genes other than CLDN16 or epigenetic factors are involved in the clinical spectrum of FHHNC; and (iii) it reinforces the variability of disease manifestation and genotype-phenotype correlations.

Entities:  

Mesh:

Year:  2011        PMID: 21633858     DOI: 10.1007/s12519-011-0295-3

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  10 in total

Review 1.  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

2.  Clinical presentation and outcome in primary familial hypomagnesaemia.

Authors:  H Shalev; M Phillip; A Galil; R Carmi; D Landau
Journal:  Arch Dis Child       Date:  1998-02       Impact factor: 3.791

Review 3.  Tight junction biology and kidney dysfunction.

Authors:  David B N Lee; Edmund Huang; Harry J Ward
Journal:  Am J Physiol Renal Physiol       Date:  2006-01

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.  Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  Stefanie Weber; Linda Schneider; Melanie Peters; Joachim Misselwitz; Gabriele Rönnefarth; Michael Böswald; Klaus E Bonzel; Tomas Seeman; Tereza Suláková; Eberhard Kuwertz-Bröking; Alojz Gregoric; Jean-Bernard Palcoux; Velibor Tasic; Friedrich Manz; Karl Schärer; Hannsjörg W Seyberth; Martin Konrad
Journal:  J Am Soc Nephrol       Date:  2001-09       Impact factor: 10.121

6.  Unusual clinical presentation and possible rescue of a novel claudin-16 mutation.

Authors:  Dominik Müller; P Jaya Kausalya; Detlef Bockenhauer; Julia Thumfart; Iwan C Meij; Michael J Dillon; William van't Hoff; Walter Hunziker
Journal:  J Clin Endocrinol Metab       Date:  2006-05-16       Impact factor: 5.958

7.  CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  Martin Konrad; Jianghui Hou; Stefanie Weber; Jörg Dötsch; Jameela A Kari; Tomas Seeman; Eberhard Kuwertz-Bröking; Amira Peco-Antic; Velibor Tasic; Katalin Dittrich; Hammad O Alshaya; Rodo O von Vigier; Sabina Gallati; Daniel A Goodenough; André Schaller
Journal:  J Am Soc Nephrol       Date:  2007-11-14       Impact factor: 10.121

8.  Disease-associated mutations affect intracellular traffic and paracellular Mg2+ transport function of Claudin-16.

Authors:  P Jaya Kausalya; Salah Amasheh; Dorothee Günzel; Henrik Wurps; Dominik Müller; Michael Fromm; Walter Hunziker
Journal:  J Clin Invest       Date:  2006-03-09       Impact factor: 14.808

9.  Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex.

Authors:  Jianghui Hou; Aparna Renigunta; Martin Konrad; Antonio S Gomes; Eveline E Schneeberger; David L Paul; Siegfried Waldegger; Daniel A Goodenough
Journal:  J Clin Invest       Date:  2008-02       Impact factor: 14.808

10.  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  M Praga; J Vara; E González-Parra; A Andrés; C Alamo; A Araque; A Ortiz; J L Rodicio
Journal:  Kidney Int       Date:  1995-05       Impact factor: 10.612

  10 in total
  10 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.  Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement.

Authors:  Félix Claverie-Martín; Rosa Vargas-Poussou; Dominik Müller; Víctor García-Nieto
Journal:  Eur J Hum Genet       Date:  2014-09-03       Impact factor: 4.246

3.  Down regulated expression of Claudin-1 and Claudin-5 and up regulation of β-catenin: association with human glioma progression.

Authors:  Hanuma K Karnati; Manas Panigrahi; Noor A Shaik; Nigel H Greig; S Appala R Bagadi; Mohammad A Kamal; Nagaiah Kapalavayi
Journal:  CNS Neurol Disord Drug Targets       Date:  2014       Impact factor: 4.388

Review 4.  Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  Mònica Vall-Palomar; Leire Madariaga; Gema Ariceta
Journal:  Pediatr Nephrol       Date:  2021-02-17       Impact factor: 3.714

5.  Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.

Authors:  Mònica Vall-Palomar; Carla Burballa; Félix Claverie-Martín; Anna Meseguer; Gema Ariceta
Journal:  J Nephrol       Date:  2021-04-30       Impact factor: 3.902

6.  Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report.

Authors:  Paulo Marcio Yamaguti; Pollyanna Almeida Costa dos Santos; Bruno Sakamoto Leal; Viviane Brandão Bandeira de Mello Santana; Juliana Forte Mazzeu; Ana Carolina Acevedo; Francisco de Assis Rocha Neves
Journal:  BMC Nephrol       Date:  2015-07-02       Impact factor: 2.388

Review 7.  The genetic framework for development of nephrolithiasis.

Authors:  Vinaya Vasudevan; Patrick Samson; Arthur D Smith; Zeph Okeke
Journal:  Asian J Urol       Date:  2016-11-28

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

9.  Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics.

Authors:  Felix Claverie-Martin
Journal:  Clin Kidney J       Date:  2015-09-01

10.  Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.

Authors:  Jingru Lu; Xiangzhong Zhao; Alessandro Paiardini; Yanhua Lang; Irene Bottillo; Leping Shao
Journal:  BMC Nephrol       Date:  2018-07-13       Impact factor: 2.388

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.