Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with a 46, XX karyotype: A case report and review of literature

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with a 46, XX karyotype: A case report and review of literature

Mayer-Rokitansky-Kuster-Hauser (MRKH) is a characteristic syndrome in which the Mullerian structures are absent or rudimentary. It is also associated with anomalies of the genitourinary and skeletal systems. Its association with gonadal dysgenesis is extremely rare and appears to be fortuitous, inde...

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Bibliographic Details
Main Authors: Kebaili, Sahbi, Chaabane, Kais, Mnif, Mouna Feki, Kamoun, Mahdi, Kacem, Faten Hadj, Guesmi, Nouha, Gassara, Hichem, Dammak, Abdallah, Louati, Doulira, Amouri, Habib, Guermazi, Mohamed
Format: Online
Language:English
Published: Medknow Publications & Media Pvt Ltd 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712384/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712384/

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