Paeds Cases · nephrology-urology-fluids-and-electrolytes
Hypokalaemia and hyperkalaemia — OSCE
OSCE communication and clinical reasoning station for the parents of a child newly diagnosed with Gitelman syndrome presenting with hypokalaemia, tetany and hypomagnesaemia, covering the diagnosis, the role of magnesium, the lifelong supplementation plan, and the safety-net.
On this page
Study tools
Target exams
Candidate brief
You are the paediatric registrar. Your daughter is 14 and has had cramps and tingling for two years, worse recently. The team has confirmed a genetic kidney condition called Gitelman syndrome. The parents want to understand what it is, whether it is curable, why their daughter needs magnesium as well as potassium, what the treatment involves day to day, and what to watch for. Explain clearly, check their understanding, and agree a plan. [9]
References3ShowHide
- [4]Viera AJ; Wouk N Potassium Disorders: Hypokalemia and Hyperkalemia. Am Fam Physician, 2015.PMID 26371733
- [9]Fulchiero R; Seo-Mayer P Bartter Syndrome and Gitelman Syndrome. Pediatr Clin North Am, 2019.PMID 30454738
- [10]Blanchard A; Bockenhauer D; Bolignano D; Calò LA Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int, 2017.PMID 28003083