First Double Vag

First Double Vag




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Related Diagnoses:
Uterine malformations
Uterus septus
Uterus duplex
Bicornuate uterus

Double vagina may be associated with several diseases including: 
Women with double vagina are likely to be affected with some other associated duplications of the reproductive tract, sumarilly called Müllerian duct anomalies. Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. Uterus is commonly affected, being either partitioned completely and existing as two separate organs (called double uterus, uterus duplex, or uterus didelphys) or only partly, creating an uterine septum (or uterus septus). 
Uterus septus (septate uterus, uterine septum)
Resulting from incomplete Müllerian duct fusion in the uterine region, a septate uterus (or uterus septus) may develop (Pic. 2). Septate uterus is the commonest uterine anomaly with a mean incidence of ~35%. The wedge-like partition may involve only the superior part of the cavity resulting in an incomplete septum or a subseptate uterus, or less frequently the total length of the cavity (complete septum) and the cervix resulting in a double cervix. It is generally accepted that having a uterine anomaly is associated with poorer pregnancy outcomes such as increased chances of spontaneous abortion, premature labor, cesarean delivery due to breech presentation, and decreased live births, compared to a normal uterus.
A bicornuate uterus or bicornate uterus, commonly referred to as a "heart-shaped" uterus, is a uterus composed of two "horns" separated by a septum. In humans, a bicornuate uterus is a type of uterine malformation. It is formed during embryogenesis, when the upper parts of the Müllerian ducts fail to fuse. As a result, the lower part of the uterus is unitary while the upper part is bifurcated.
Uterus duplex (uterus didelphys, double uterus)
Uterus duplex (or uterus didelphys) represents a uterine malformation where the uterus is present as a paired organ when the embryogenetic fusion of the Müllerian ducts fails to occur (Pic. 3). A didelphys uterus is one of the least common among MDAs. Most women with a didelphys uterus are asymptomatic, but some present with dyspareunia or dysmenorrhea in the presence of a varying degree of longitudinal vaginal septum. Rarely, genital neoplasms, hematocolpos/hematometrocolpos (a collection or retention of blood in the vagina and/or in the uterine cavity), and renal anomalies are reported in association with didelphys uterus. Despite some of these complications, there are many cases of women with a didelphys uterus that did not exhibit any reproductive or gestational challenges.

“ Uterine septum ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Bicornuate uterus ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Didelphys Uterus: A Case Report and Review of the Literature ”

―by Rezai et al.

licensed under

CC BY 3.0




“ Uterus didelphys ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Intrapartum Diagnosis and Treatment of Longitudinal Vaginal Septum ”

―by de Franca Neto et al.

licensed under

CC BY 3.0




“ Vaginal septum ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ A_system_of_gynecology_(1887)_(14802859803) ”

―by Internet Archive Book Images

licensed under

CC BY-SA 3.0




“ Operative_gynecology_-_(1906)_(14760507606).jpg ”

―by Internet Archive Book Images

licensed under

CC BY-SA 3.0




“ Uterus didelphys ”

―by Internet Archive Book Images

licensed under

no known copyright restrictions



Except where otherwise noted, content on this site is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License , involving multiple copyrights under different terms listed in the Sources section.

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Double vagina, synonimically called longitudinal vaginal septum, is a congenital abnormality of the female reproductive tract. During embryonic development, a vagina is usually formed by the fusion of two tubes, called Müllerian ducts. If they fail to fuse in the vertical plane, the longitudinal vaginal septum develops, resulting in a double vagina (Pic. 1). There may be associated duplications of the more cranial parts of the Müllerian derivatives, a double cervix, and either a uterine septum or uterus didelphys (double uterus). 
The person with a longitudinal vaginal septum may be asymptomatic and not aware of the condition. It may present clinically as a difficulty in inserting tampons, persistent bleeding despite the presence of a tampon, or dyspareunia (pain felt during sexual intercourse). Women with this condition have also an increased risk of pregnancy and delivery complications, such as early pregnancy loss, miscarriage and premature labor.
A type of female genital malformation resulting from an abnormal development of the Müllerian duct(s) during embryogenesis.
A form of a congenital malformation where the uterine cavity is partitioned by a longitudinal septum. It is one of Müllerian duct anomalies.
Congenital uterine malformation where both Müllerian ducts develop but fail to fuse, thus the woman has a "double uterus".
Inborn morphological deviation of the uterus - one of the Müllerian duct anomalies where the uterine cavity is divided in the upper part.







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Related Diagnoses:
Uterine malformations
Uterus septus
Uterus duplex
Bicornuate uterus

Double vagina may be associated with several diseases including: 
Women with double vagina are likely to be affected with some other associated duplications of the reproductive tract, sumarilly called Müllerian duct anomalies. Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. Uterus is commonly affected, being either partitioned completely and existing as two separate organs (called double uterus, uterus duplex, or uterus didelphys) or only partly, creating an uterine septum (or uterus septus). 
Uterus septus (septate uterus, uterine septum)
Resulting from incomplete Müllerian duct fusion in the uterine region, a septate uterus (or uterus septus) may develop (Pic. 2). Septate uterus is the commonest uterine anomaly with a mean incidence of ~35%. The wedge-like partition may involve only the superior part of the cavity resulting in an incomplete septum or a subseptate uterus, or less frequently the total length of the cavity (complete septum) and the cervix resulting in a double cervix. It is generally accepted that having a uterine anomaly is associated with poorer pregnancy outcomes such as increased chances of spontaneous abortion, premature labor, cesarean delivery due to breech presentation, and decreased live births, compared to a normal uterus.
A bicornuate uterus or bicornate uterus, commonly referred to as a "heart-shaped" uterus, is a uterus composed of two "horns" separated by a septum. In humans, a bicornuate uterus is a type of uterine malformation. It is formed during embryogenesis, when the upper parts of the Müllerian ducts fail to fuse. As a result, the lower part of the uterus is unitary while the upper part is bifurcated.
Uterus duplex (uterus didelphys, double uterus)
Uterus duplex (or uterus didelphys) represents a uterine malformation where the uterus is present as a paired organ when the embryogenetic fusion of the Müllerian ducts fails to occur (Pic. 3). A didelphys uterus is one of the least common among MDAs. Most women with a didelphys uterus are asymptomatic, but some present with dyspareunia or dysmenorrhea in the presence of a varying degree of longitudinal vaginal septum. Rarely, genital neoplasms, hematocolpos/hematometrocolpos (a collection or retention of blood in the vagina and/or in the uterine cavity), and renal anomalies are reported in association with didelphys uterus. Despite some of these complications, there are many cases of women with a didelphys uterus that did not exhibit any reproductive or gestational challenges.

“ Uterine septum ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Bicornuate uterus ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Didelphys Uterus: A Case Report and Review of the Literature ”

―by Rezai et al.

licensed under

CC BY 3.0




“ Uterus didelphys ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ Intrapartum Diagnosis and Treatment of Longitudinal Vaginal Septum ”

―by de Franca Neto et al.

licensed under

CC BY 3.0




“ Vaginal septum ”

―sourced from Wikipedia

licensed under

CC BY-SA 3.0




“ A_system_of_gynecology_(1887)_(14802859803) ”

―by Internet Archive Book Images

licensed under

CC BY-SA 3.0




“ Operative_gynecology_-_(1906)_(14760507606).jpg ”

―by Internet Archive Book Images

licensed under

CC BY-SA 3.0




“ Uterus didelphys ”

―by Internet Archive Book Images

licensed under

no known copyright restrictions



Except where otherwise noted, content on this site is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License , involving multiple copyrights under different terms listed in the Sources section.

For patients





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Self-diagnosis





Therapies





Education Zone





About





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Stay informed



Feedback: Help make Fertilitypedia better.





Fertilitypedia would like to thank the following sponsors for making this site possible



© 2022 Fertilitypedia.org



Terms of use



To improve your experience on this site we use cookies. Please read our Terms of Use for more information. OK
Double vagina, synonimically called longitudinal vaginal septum, is a congenital abnormality of the female reproductive tract. During embryonic development, a vagina is usually formed by the fusion of two tubes, called Müllerian ducts. If they fail to fuse in the vertical plane, the longitudinal vaginal septum develops, resulting in a double vagina (Pic. 1). There may be associated duplications of the more cranial parts of the Müllerian derivatives, a double cervix, and either a uterine septum or uterus didelphys (double uterus). 
The person with a longitudinal vaginal septum may be asymptomatic and not aware of the condition. It may present clinically as a difficulty in inserting tampons, persistent bleeding despite the presence of a tampon, or dyspareunia (pain felt during sexual intercourse). Women with this condition have also an increased risk of pregnancy and delivery complications, such as early pregnancy loss, miscarriage and premature labor.
A type of female genital malformation resulting from an abnormal development of the Müllerian duct(s) during embryogenesis.
A form of a congenital malformation where the uterine cavity is partitioned by a longitudinal septum. It is one of Müllerian duct anomalies.
Congenital uterine malformation where both Müllerian ducts develop but fail to fuse, thus the woman has a "double uterus".
Inborn morphological deviation of the uterus - one of the Müllerian duct anomalies where the uterine cavity is divided in the upper part.

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The story "Drunken Muse" was audio recorded on a hidden voice recorder during the conversations about two decades ago. The story-teller didn't know or consent to the recording.
The audio tapes on compact cassettes were never used. The records were partially damaged and lost.
Herewith the unedited transcript version.
I am so pumped to get back to painting as I return to the second year of the art school after a full year suspension. As always it is like time-travel culturally speaking, like walking right into the middle ages going through the antique building’s portal.
Art studios are the huge L-shaped lofts with super tall ceilings 20 feet no less with the wall to wall windows so that sunlight illuminates the space from south and east side designed for the purpose so that one could paint there from morning till sunset.
In a studio there are classical gypsum sculptures, expensive copies of Venus de Milo, David, Laocoön and the others. In the art studio there stood the noses, eyes, lips, feet, and palms on the wood shelves.
Sketching the gypsum body parts helps you to build the classic academic base on which stands the whole modern and contempo art. This sort of teaching is specific for the art schools that preserve the traditions they had been founded on. There is only few art schools like this and of this caliber left now. Could be that this is the only legendary school that continues to function as if nothing had changed in the world. In the rest of the world with billions of some art classes nobody knows
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