Article
Gitelman syndrome and primary hyperparathyroidism: a rare association.
BMJ case reports - 5 Jun 2018
Rego Teresa, Fonseca Fernando, Cerqueira Rita, Agapito Ana
Abstract excerpt
Gitelman syndrome(GS) is a rare autosomal recessive salt-losing tubulopathy of young adults, characterised by hypokalaemia, hypomagnesaemia, hypocalciuria and secondary hyperaldosteronism. Hypercalcaemia due to hypocalciuria in these patients is extremely rare.A 25-year-old healthy woman was referred to the Endocrinology clinic for evaluation of persistent hypokalaemia. She presented with fatigue, myalgias,...
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