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This device is not only portable, but also can monitor the metabolic status of patients in real time, providing clinicians with a rapid basis for diagnosis

The hyperkalemia associated with Gordon syndrome is due to the fact that WNK1 and WNK4 normally activate the renal outer medullary K + channel (ROMK, encoded by the KCNJ1 gene) present in the apical membranes of late distal convoluted tubule (DCT2) cells and connecting tubule cells