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Deletion of exons 2-4 in the BSND gene causes severe antenatal Bartter syndrome.
Bircan, Zelal; Harputluoglu, Filiz; Jeck, Nikola.
Afiliação
  • Bircan Z; Department of Pediatric Nephrology, Kocaeli University Hospital, 41380 Umuttepe, Kocaeli, Turkey. zbircan@superonline.com
Pediatr Nephrol ; 24(4): 841-4, 2009 Apr.
Article em En | MEDLINE | ID: mdl-18843510
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bartter / Deleção de Sequência / Canais de Cloreto / Predisposição Genética para Doença Tipo de estudo: Etiology_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bartter / Deleção de Sequência / Canais de Cloreto / Predisposição Genética para Doença Tipo de estudo: Etiology_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2009 Tipo de documento: Article