[Gitelman's Syndrome: from diagnosis to follow-up during pregnancy].

  title={[Gitelman's Syndrome: from diagnosis to follow-up during pregnancy].},
  author={Rafael Brito Foureaux Ribeiro and S{\'e}rgio Ant{\^o}nio Dias da Silveira Junior and Cristiane Calaça Borges Silva and Gisele Rodrigues Gontijo},
  journal={Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia},
  volume={37 2},
Gitelman's Syndrome (GS) is a rare autosomal recessive salt-wasting nephropathy, classically characterized by hypokalemia, hypomagnesemia, hypocalciuria, metabolic alkalosis and low blood pressure. Fatigue, muscle weakness and muscle paralysis are common symptoms. Besides the typical electrolyte disturbances, others laboratory findings include… CONTINUE READING