An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report.
Yuki IshinodaAsuka UtoYoshifumi YamadaMaki OkazakiHidetomo AsadaSeina WakamatsuIsao KuriharaHironori ShibataTomohiro IshiiTomonobu HasegawaHiroo KumagaiAkira KasugaPublished in: BMC endocrine disorders (2022)
17OHD can resemble PA. The combination of a high ARR and low cortisol level should trigger the consideration of 17OHD.