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Table 2 Clinical features in all patients

From: Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene

Clinical feature Case 1 (index) Case 2 Case 3 Case 4
Age in years on presentation/follow up 14 8 11 8
Gender Female Male Female Female
Weight centile on presentation/follow up 75th/90th <5th/10th 15th 50th
Height centile on presentation/follow up 50th/75th 30th 10th 30th
History of polyuria and polydipsia Negative Negative Negative Negative
Blood pressure 114/75 100/70 110/68 105/68
Nephrocalcinosis/Nephrolithiasis Negative Negative Negative Negative