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

Falhammar, H; Torpy, D J

Falhammar, H; Torpy, D J.

Affiliation

Falhammar H; Menzies School of Health Research, Royal Darwin Hospital, Darwin, Northern Territory, Australia.
Torpy DJ; Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital, Stockholm, Sweden.

Intern Med J ; 46(9): 1115-6, 2016 Sep.

Article in En | MEDLINE | ID: mdl-27633475

Subject(s)

Adrenal Gland Neoplasms/diagnostic imaging; Adrenal Gland Neoplasms/genetics; Adrenal Hyperplasia, Congenital/complications; Steroid 21-Hydroxylase/genetics; Abdomen/diagnostic imaging; Adult; Humans; Male; Mutation; Tomography, X-Ray Computed

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Adrenal Gland Neoplasms / Adrenal Hyperplasia, Congenital Limits: Adult / Humans / Male Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2016 Type: Article Affiliation country: Australia

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