A 42-year-old man presented with adrenal incidentaloma due to non-classic congenital adrenal hyperplasia with a novel CYP21A2 mutation

被引：4
作者：
Falhammar, H. [1 ,4 ,5 ]
Torpy, D. J. [2 ,3 ]
机构：
[1] Royal Darwin Hosp, Menzies Sch Hlth Res, Darwin, NT, Australia
[2] Royal Adelaide Hosp, Endocrine & Metab Unit, Adelaide, SA, Australia
[3] Univ Adelaide, Adelaide, SA, Australia
[4] Karolinska Univ Hosp, Dept Endocrinol Metab & Diabet, Stockholm, Sweden
[5] Karolinska Inst, Dept Mol Med & Surg, Guidlelines, Stockholm, Sweden
来源：
INTERNAL MEDICINE JOURNAL | 2016年 / 46卷 / 09期
关键词：
21-HYDROXYLASE DEFICIENCY; DIAGNOSIS;
D O I：
10.1111/imj.13177
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：1115 / 1116
页数：2
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