Literature DB >> 23732434

Late presentation of simple virilising 21-hydroxylase deficiency in a Chinese woman with Turner's syndrome.

K F Lee1, Angel O K Chan, Juliana M C Fok, Maria W H Mak, K C Yu, K M Lee, C C Shek.   

Abstract

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency is a well-known disorder of sexual development (previously known as ambiguous genitalia) in genotypic female neonates. We report on a 66-year-old Chinese, brought up as male, with a simple virilising form of congenital adrenal hyperplasia associated with Turner's syndrome (karyotype 45,X/47,XXX/46,XX). His late presentation was recognised due to his exceptionally short stature and persistent sexual ambiguity. His condition was only brought to medical attention as he developed a huge abdominal mass, which later turned out to be a benign ovarian mucinous cyst. It is therefore important to look out for co-existing congenital adrenal hyperplasia in patients with Turner's syndrome and virilisation, after the presence of Y chromosome material has been excluded.

Entities:  

Keywords:  Adrenal hyperplasia, congenital; Steroids/urine; Turner syndrome; Virilism

Mesh:

Year:  2013        PMID: 23732434     DOI: 10.12809/hkmj133717

Source DB:  PubMed          Journal:  Hong Kong Med J        ISSN: 1024-2708            Impact factor:   2.227


  2 in total

1.  Turner syndrome with positive SRY gene and non-classical congenital adrenal hyperplasia: A case report.

Authors:  Mei-Nan He; Shan-Chao Zhao; Ji-Min Li; Lu-Lu Tong; Xin-Zhao Fan; Yao-Ming Xue; Xiao-Hong Lin; Ying Cao
Journal:  World J Clin Cases       Date:  2021-04-06       Impact factor: 1.337

2.  Teaching and Learning Medical Biochemistry: Perspectives from a Student and an Educator.

Authors:  Mehdi Afshar; Zhiyong Han
Journal:  Med Sci Educ       Date:  2014
  2 in total

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