Acute abdomen in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome
Background. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a malformation of female genital tract (incidence 1 in 4000 female newborn children). It appears as a result of a disorder in the development of Millerian cannals. Etiology is unknown. Syndrome MRKH is the most frequent cause of primary a...
Main Authors: | Petrić Aleksandra, Stefanović Milan, Vukomanović Predrag, Živadinović Radomir, Tubić Aleksandra, Janjić Zoran |
---|---|
Format: | Article |
Language: | English |
Published: |
Military Health Department, Ministry of Defance, Serbia
2008-01-01
|
Series: | Vojnosanitetski Pregled |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0042-8450/2008/0042-84500809706P.pdf |
Similar Items
-
A rare case of Mayer-Rokitansky-Kuster-Hauser syndrome with multiple leiomyomas in hypoplastic uterus
by: Maithili Mandar Kulkarni, et al.
Published: (2015-01-01) -
Leiomyoma development in Mayer-Rokitansky-Küster-Hauser syndrome: a case report and a narrative review of the literature
by: Nikolaos Blontzos, et al.
Published: (2019-07-01) -
Mayer-Rokitansky-Kuster-Hauser Syndrome
by: Shy, Hannah Marie
Published: (2016) -
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: A Case Report
by: Jadhav Mayuri, et al.
Published: (2014-03-01) -
A Case of Mayer–Rokitansky–Küster–Hauser Syndrome with a Fused Pancake-shaped Pelvic Kidney
by: Ali Reza Eftekhari Moghadam, et al.
Published: (2019-01-01)