Severe hypertension caused by 17α-hydroxylase deficiency: A case report.

Background: 17α-hydroxylase deficiency (17OHD) is an autosomal recessive genetic disease characterized by low renin hypertension, abnormal sexual development, and reduced androgen levels. The morbidity rate of 17OHD is less than 1/10,000, and a lack of knowledge of this condition may lead to misdiagnosis and delayed treatment.

Case Presentation: This is a case report of a patient suffering from hypertension who was diagnosed with 17OHD.