hrp0092p3-322 | Late Breaking Abstracts | ESPE2019
Hashim Raihana
, Atapattu Navoda
, Fernando Jerard
, Prematilake Dilusha
, Gunasekara Buddi
, Suntharesan Janani
, De Silva Dimarsha
Introduction: Bartter syndrome (BS) is a rare genetic renal tubular disorder characterized by hypokalemia, salt-wasting and metabolic alkalosis. Polyuria, polydipsia, hypokalemia and salt loss are responsible for the growth retardation seen in BS. Persistent growth failure despite optimizing medical therapy may be due to growth hormone (GH) deficiency.Case diagnosis and treatment: A 9-year-old girl diagnosed with Bartter...