Article

Complications and treatment of hypercalciuria in patients affected by Familial Hyperkalemic Hypertension (FHHt)

2024-03-10

Abstract excerpt

<h4>Background and hypothesis</h4> Gordon syndrome (also pseudohypoaldosteronism type II (PHAII) or Familial Hyperkalemia with Hypertension (FHHt)) is a genetic condition characterised by hypertension, hyperkalaemia, hyperchloraemic metabolic acidosis and hypercalciuria caused by an activation of the thiazide-sensitive sodium-chloride cotransporter (NCC, encoded by SLC12A3 ) in the distal convoluted tubule of the...

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Literature Corpus work: e25d906e-172a-5c73-bc13-f5368ab2589e
DOI: 10.1101/2024.03.09.24303922

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