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The journal Journal of Pediatric Endocrinology and Metabolism has published an article about Gordon syndrome. Gordon syndrome (GS) is a rare form of monogenic hypertension characterized by low renin hypertension, hyperkalemia, hyperchloremic metabolic acidosis, and normal glomerular filtration rate. To date, four genes causing GS have been identified as: WNK1, WNK4, CUL3, and KLHL3. The full-text article you can find here.