ea0021p84 | Clinical practice/governance and case reports | SFEBES2009
Balaguruswamy Saravanan
, Chandrasekara W M H S
, Rao Sandhya
, Furlong Niall
, Abdalla Tarig
Gitelmans syndrome (GS) is a rare autosomal recessive renal tubular disorder caused by defects of thiazide sensitive Na-Cl co-transporter due to mutations of the SLC12A3 gene.We report a case of a 23-year-old woman, who presented with excessive tiredness in her second pregnancy. She had a past history of hypokalaemia in a previous pregnancy (attributed to vomiting), which required multiple admissions for i.v. potassium replacement despi...