Mullerian dysgenesis: Difference between revisions
No edit summary |
No edit summary |
||
Line 14: | Line 14: | ||
}} | }} | ||
{{SI}} | {{SI}} | ||
{{CMG}} | |||
{{Editor Help}} | {{Editor Help}} |
Revision as of 20:59, 9 January 2009
Mullerian dysgenesis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Related Key Words and Synonyms: uterus, uterine, female reproductive tract, müllerian congenital uterine anomalies, müllerian anomalies, müllerian duct anomalies, Mayer-Rokitansky-Kuster-Hauser syndrome, female reproductive tract developmental abnormalities, paramesonephric developmental abnormalities
Müllerian duct anomalies are an infrequent cause of infertility that is often treatable.
Müllerian duct anomalies are associated with:
- Higher incidence of infertility
- Repeated first trimester spontaneous abortions
- Fetal intrauterine growth retardation
- Fetal malposition
- Preterm labor
- Retained placenta
Acknowledgements
The content on this page was first contributed by: C. Michael Gibson, M.S., M.D.