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

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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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/
http://irep.iium.edu.my/33545/1/79-279-1-PB.pdf
id iium-33545
recordtype eprints
spelling iium-335452013-12-19T06:31:57Z http://irep.iium.edu.my/33545/ A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis Shahar, Mohamed Arif Omar , Ahmad Marzuki Sukor, Norlela Abd Wahab, Norasyikin Zainuddin, Suehazlyn Mustafa, Norlaila Kamaruddin, Nor Azmi R Medicine (General) RC Internal medicine 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 the spectrum of streak ovary to normal and polycystic ovary (PCO) in relation to the X chromosome in TS. We herewith report the first case of mosaic Turner karyotype clustering with empty sella, pituitary atrophy, müllerian dysgenesis and single PCO. Malaysian Endocrine and Metabolic Society 2013 Article PeerReviewed application/pdf en http://irep.iium.edu.my/33545/1/79-279-1-PB.pdf Shahar, Mohamed Arif and Omar , Ahmad Marzuki and Sukor, Norlela and Abd Wahab, Norasyikin and Zainuddin, Suehazlyn and Mustafa, Norlaila and Kamaruddin, Nor Azmi (2013) A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis. Journal of Endocrinology and Metabolism, 3 (1). pp. 62-66. ISSN 2229-9572 http://www.jmems.org/index.php/jmems/article/view/79
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic R Medicine (General)
RC Internal medicine
spellingShingle R Medicine (General)
RC Internal medicine
Shahar, Mohamed Arif
Omar , Ahmad Marzuki
Sukor, Norlela
Abd Wahab, Norasyikin
Zainuddin, Suehazlyn
Mustafa, Norlaila
Kamaruddin, Nor Azmi
A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
description 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 the spectrum of streak ovary to normal and polycystic ovary (PCO) in relation to the X chromosome in TS. We herewith report the first case of mosaic Turner karyotype clustering with empty sella, pituitary atrophy, müllerian dysgenesis and single PCO.
format Article
author Shahar, Mohamed Arif
Omar , Ahmad Marzuki
Sukor, Norlela
Abd Wahab, Norasyikin
Zainuddin, Suehazlyn
Mustafa, Norlaila
Kamaruddin, Nor Azmi
author_facet Shahar, Mohamed Arif
Omar , Ahmad Marzuki
Sukor, Norlela
Abd Wahab, Norasyikin
Zainuddin, Suehazlyn
Mustafa, Norlaila
Kamaruddin, Nor Azmi
author_sort Shahar, Mohamed Arif
title A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
title_short A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
title_full A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
title_fullStr A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
title_full_unstemmed A rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
title_sort rare case of polycystic ovarian syndrome, empty sella and pituitary atrophy in a patient with mosaic turner karyotype and mullerian dysgenesis
publisher Malaysian Endocrine and Metabolic Society
publishDate 2013
url http://irep.iium.edu.my/33545/
http://irep.iium.edu.my/33545/
http://irep.iium.edu.my/33545/1/79-279-1-PB.pdf
first_indexed 2023-09-18T20:48:29Z
last_indexed 2023-09-18T20:48:29Z
_version_ 1777409835659165696

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