A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis

• 主要な著者: Shahar, Mohamed Arif, Omar , Ahmad Marzuki, Sukor, Norlela, Abd Wahab, Norasyikin, Zainuddin, Suehazlyn, Mustafa, Norlaila, Kamaruddin, Nor Azmi
• フォーマット: 論文
• 言語: English
• 出版事項: Malaysian Endocrine and Metabolic Society 2013
• 主題: R Medicine (General); RC Internal medicine
• オンライン･アクセス: http://irep.iium.edu.my/33545/1/79-279-1-PB.pdf; http://irep.iium.edu.my/33545/; http://www.jmems.org/index.php/jmems/article/view/79

An 18-year-old lady presented with primary amenorrheoa and was later confirmed to have mosiac Turner karyotype. The presence of müllerian dysgenesis in the spectrum of uterine agenesis to uterine atrophy has been demonstrated in Turner syndrome (TS) before. Similarly, previous study has described th...