Mullerian agenesis : presenting as an isolated rudimentary uterus
Joint Authors
al-Kabi, Jumah
al-Zahiri, Sharina
Aswad, Sad
Langer, Ruth D.
Suid, Abd al-Qadir
Source
Issue
Vol. 29, Issue 5 (31 Oct. 2014)2 p.
Publisher
Publication Date
2014-10-31
Country of Publication
Oman
No. of Pages
2
Main Subjects
Abstract EN
Müllerian agenesis (Mayer-Rokitansky-Küster-Hauser syndrome) is typically described as missing uterus and fallopian tubes with malformation of the upper vagina.
Isolated uterine anomaly is a rare variant of the syndrome.
A 16-year-old female with primary amenorrhea and rudimentary uterus on the magnetic resonance imaging (MRI) was reported.
The ovaries, vaginal canal and other abdominal and pelvic organs were normal.
The patient’s sexual, physical and developmental characteristics were normal.
The serum follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol, prolactin, testosterone and thyroid-stimulating hormone (TSH) were also normal.
Thus, this patient represents an important variant of the Müllerian agenesis syndrome.
American Psychological Association (APA)
al-Zahiri, Sharina& al-Kabi, Jumah& Aswad, Sad& Suid, Abd al-Qadir& Langer, Ruth D.. 2014. Mullerian agenesis : presenting as an isolated rudimentary uterus. Oman Medical Journal،Vol. 29, no. 5.
https://search.emarefa.net/detail/BIM-908145
Modern Language Association (MLA)
al-Zahiri, Sharina…[et al.]. Mullerian agenesis : presenting as an isolated rudimentary uterus. Oman Medical Journal Vol. 29, no. 5 (2014).
https://search.emarefa.net/detail/BIM-908145
American Medical Association (AMA)
al-Zahiri, Sharina& al-Kabi, Jumah& Aswad, Sad& Suid, Abd al-Qadir& Langer, Ruth D.. Mullerian agenesis : presenting as an isolated rudimentary uterus. Oman Medical Journal. 2014. Vol. 29, no. 5.
https://search.emarefa.net/detail/BIM-908145
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-908145