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X-linked congenital adrenal hypoplasia: a case presentation.
Ouyang, Hong; Chen, Bo; Wu, Na; Li, Ling; Du, Runyu; Qian, Meichen; Yu, Wenshu; He, Yujing; Liu, Xinyan.
Affiliation
  • Ouyang H; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
  • Chen B; Department of Endocrinology, The First People's Hospital of Kerqin District, Tongliao, Inner Mongolia, China.
  • Wu N; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China. 3441535223@qq.com.
  • Li L; Clinical Skills Practice Teaching Center, Shengjing Hospital of China Medical University, Shenyang, China. 3441535223@qq.com.
  • Du R; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
  • Qian M; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
  • Yu W; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
  • He Y; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
  • Liu X; Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, China.
BMC Endocr Disord ; 21(1): 118, 2021 Jun 15.
Article in En | MEDLINE | ID: mdl-34130666

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adrenal Hyperplasia, Congenital / Genetic Diseases, X-Linked / DAX-1 Orphan Nuclear Receptor / Hypoadrenocorticism, Familial / Hypogonadism / Mutation Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: BMC Endocr Disord Year: 2021 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adrenal Hyperplasia, Congenital / Genetic Diseases, X-Linked / DAX-1 Orphan Nuclear Receptor / Hypoadrenocorticism, Familial / Hypogonadism / Mutation Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: BMC Endocr Disord Year: 2021 Type: Article Affiliation country: China