Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family.
Yan JiangJ DuY-W SongW-B WangQ-Q PangM LiO WangX-L LianX-P XingW-B XiaPublished in: Journal of endocrinological investigation (2019)
The present findings supported that the Bartter-like hypokalemia is a new complication of PHOAR2 caused by the high level of PGE2. Etoricoxib was demonstrated to be effective for the renal hypokalemia in PHO patients.