Clinical and diagnostic features of Bartter and Gitelman syndromes.

Journal: Clinical kidney journal
Published Date: Nov 10, 2017

Abstract

BACKGROUND: Bartter and Gitelman syndromes are autosomal recessive disorders of renal tubular salt handling. Due to their rarity, limited long-term data are available to inform prognosis and management.

Authors

  • Patrick R Walsh
    Department of Nephrology, Great North Children's Hospital NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Yincent Tse
    Department of Nephrology, Great North Children's Hospital NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Emma Ashton
    North East Thames Regional Genetics Service Laboratories, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Daniela Iancu
    North East Thames Regional Genetics Service Laboratories, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Lucy Jenkins
    Department of Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Marc Bienias
    Department of Paediatrics, Medical Faculty Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
  • Robert Kleta
    Department of Pediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • William Van't Hoff
    Department of Pediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Detlef Bockenhauer
    Department of Pediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

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