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

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

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...

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Bibliographic Details
Main Authors:	Shahar, Mohamed Arif, Omar , Ahmad Marzuki, Sukor, Norlela, Abd Wahab, Norasyikin, Zainuddin, Suehazlyn, Mustafa, Norlaila, Kamaruddin, Nor Azmi
Format:	Article
Language:	English
Published:	Malaysian Endocrine and Metabolic Society 2013
Subjects:	R Medicine (General) RC Internal medicine
Online Access:	http://irep.iium.edu.my/33545/ http://irep.iium.edu.my/33545/1/79-279-1-PB.pdf

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