Literature DB >> 18843510

Deletion of exons 2-4 in the BSND gene causes severe antenatal Bartter syndrome.

Zelal Bircan1, Filiz Harputluoglu, Nikola Jeck.   

Abstract

BSND gene mutations usually cause severe forms of antenatal Bartter syndrome and sensorineural deafness (SND). Chronic renal failure and transient hypercalciuria are reported as controversial symptoms of this syndrome. All twelve reported BSND mutations cause SND, whereas only two of the mutations give rise to normal glomerular filtration rate (GFR) and two other mutations cause hypercalciuria. The case we report here, where the patient presented with severe clinical symptoms and deletion on exons 2-4 of the BSND gene, has not been reported previously. Decreased GFR, along with hypercalciuria and difficulties in managing fluid and electrolyte requirements, are the reasons why this patient was brought to attention.

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Year:  2008        PMID: 18843510     DOI: 10.1007/s00467-008-1008-6

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


  18 in total

1.  Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

Authors:  M Vollmer; N Jeck; H H Lemmink; R Vargas; D Feldmann; M Konrad; F Beekmann; L P van Den Heuvel; G Deschenes; L M Guay-Woodford; C Antignac; H W Seyberth; F Hildebrandt; N V Knoers
Journal:  Nephrol Dial Transplant       Date:  2000-07       Impact factor: 5.992

2.  Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.

Authors:  Ferda Ozlu; Hacer Yapicioğlu; Mehmet Satar; Nejat Narli; Kenan Ozcan; Mithat Buyukcelik; Martin Konrad; Osman Demirhan
Journal:  Pediatr Nephrol       Date:  2006-05-24       Impact factor: 3.714

3.  A compound heterozygous mutation in the BSND gene detected in Bartter syndrome type IV.

Authors:  Sachiko Kitanaka; Utako Sato; Kenichi Maruyama; Takashi Igarashi
Journal:  Pediatr Nephrol       Date:  2005-12-03       Impact factor: 3.714

4.  Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

Authors:  T M Brennan; D Landau; H Shalev; F Lamb; B C Schutte; R Y Walder; A L Mark; R Carmi; V C Sheffield
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

5.  Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder.

Authors:  D Landau; H Shalev; M Ohaly; R Carmi
Journal:  Am J Med Genet       Date:  1995-12-04

6.  Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families.

Authors:  Víctor García-Nieto; Carlos Flores; Maria I Luis-Yanes; Eduardo Gallego; Jesús Villar; Félix Claverie-Martín
Journal:  Pediatr Nephrol       Date:  2006-03-29       Impact factor: 3.714

7.  Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies.

Authors:  Cinzia Cortesi; Alberto Bettinelli; Francesco Emma; Michel Fischbach; Paolo Bertolani; Mario G Bianchetti
Journal:  Nephrol Dial Transplant       Date:  2005-06-28       Impact factor: 5.992

8.  The neonatal variant of Bartter syndrome and deafness: preservation of renal function.

Authors:  Hanna Shalev; Melly Ohali; Leonid Kachko; Daniel Landau
Journal:  Pediatrics       Date:  2003-09       Impact factor: 7.124

9.  Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

Authors:  K Nozu; T Inagaki; X J Fu; Y Nozu; H Kaito; K Kanda; T Sekine; T Igarashi; K Nakanishi; N Yoshikawa; K Iijima; M Matsuo
Journal:  J Med Genet       Date:  2008-03       Impact factor: 6.318

Review 10.  Recent advances in molecular genetics of hereditary magnesium-losing disorders.

Authors:  Martin Konrad; Stefanie Weber
Journal:  J Am Soc Nephrol       Date:  2003-01       Impact factor: 10.121

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