11β-羟化酶缺陷症合并亚急性甲状腺炎致严重低血钾1例报道及文献复习

11β-Hydroxylase deficiency combined with subacute thyroiditis resulting in severe hypokalemia: A case report and literature review

11β-羟化酶缺陷症(11β-hydroxylase deficiency, 11β-OHD)是常染色体隐性遗传性疾病先天性肾上腺皮质增生症中相对少见的一个类型, 本文报道了我院收治的1例11β-OHD合并亚急性甲状腺炎致严重低血钾的诊治情况并复习相关文献。

11β-Hydroxylase deficiency(11β-OHD)is a relatively rare type of autosomal recessive hereditary disease congenital adrenal cortical hyperplasia.This article reports the diagnosis and treatment of a case of 11β-OHD combined with subacute thyroiditis leading to severe hypokalemia treated in our hospital,along with a review of relevant literature.