Literature DB >> 25410674

Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Ernesto Martin-Nuñez1, Elizabeth Cordoba-Lanus, Hilaria Gonzalez-Acosta, Aniana Oliet, Elvira Izquierdo, Felix Claverie-Martin.   

Abstract

BACKGROUND: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal recessive tubular disease caused by mutations in the CLDN16 or CLDN19 gene. Previous studies using microsatellite markers flanking the CLDN19 locus estimated that p.G20D (c.59G>A), a recurrent mutation in Spanish families, is a founder mutation. In the present study, we assessed the haplotype of Spanish patients using single nucleotide polymorphisms (SNPs).
METHODS: Twenty-seven FHHNC patients were included in this study. We analyzed four SNPs located in CLDN19 introns 3 and 4 by polymerase chain reaction amplification and DNA sequencing.
RESULTS: Three new patients with homozygous p.G20D were identified. The SNP genotyping analysis showed that alleles carrying this mutation shared a common SNP haplotype.
CONCLUSIONS: Our findings suggest the existence of a founder effect responsible for FHHNC in our cohort. Testing for the presence of mutation p.G20D should be the first genetic screening in Spanish patients.

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Year:  2014        PMID: 25410674     DOI: 10.1007/s12519-014-0528-3

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


  15 in total

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

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

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Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-24       Impact factor: 11.205

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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.  Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Authors:  Félix Claverie-Martín; Víctor García-Nieto; Cesar Loris; Gema Ariceta; Inmaculada Nadal; Laura Espinosa; Ángeles Fernández-Maseda; Montserrat Antón-Gamero; Africa Avila; Álvaro Madrid; Hilaria González-Acosta; Elizabeth Córdoba-Lanus; Fernando Santos; Marta Gil-Calvo; Mar Espino; Elena García-Martinez; Ana Sanchez; Rafael Muley
Journal:  PLoS One       Date:  2013-01-03       Impact factor: 3.240

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  5 in total

Review 1.  Claudins in Renal Physiology and Pathology.

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3.  Establishment of urinary exosome-like vesicles isolation protocol for FHHNC patients and evaluation of different exosomal RNA extraction methods.

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4.  Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.

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Journal:  J Clin Lab Anal       Date:  2019-09-10       Impact factor: 2.352

5.  Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

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  5 in total

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