Relevant bibliographies by topics / Mullerian duct

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Mullerian duct'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Mullerian duct.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Mullerian duct"

1

Niranjan, Richa, A. K. Singh, and Anjoo Yadav. "Embryological basis of malformed female genital tract and various classifications." National Journal of Clinical Anatomy 03, no. 03 (2014): 150–58. http://dx.doi.org/10.1055/s-0039-3401756.

Full text
Abstract:
AbstractDevelopmental anomalies of the Mullerian duct system represent some of the most fascinating disorders that obstetricians and gynaecologists encounter. The uterus is formed during embryogenesis by the fusion of the two paramesonephric ducts (Mullerian ducts). This process usually fuses the two Mullerian ducts into a single uterine body, but fails to take place in the affected women who maintain their double Mullerian systems. A bicornuate uterus is a type of a uterine malformation where upper part of uterus forms two horns. The fusion process of upper part of Mullerian duct is altered.
APA, Harvard, Vancouver, ISO, and other styles
2

Izhar, Shabnam, Purnima Singh, and Kusum Gupta. "Persistent Mullerian Duct Syndrome." Annals of Pathology and Laboratory Medicine 6, no. 8 (2019): C91–93. http://dx.doi.org/10.21276/apalm.2559.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Dr., Labiha Ayesha Shaikh Fayazoddin1 Dr. Gopal Rathi2 Dr. Ashutosh Chitnis3 Dr. Gayatri Patil4. "A case series of mullerian duct anomalies – Diagnostic Journey." International Journal of Medical Science in Clinical Research and Review 8, no. 02 (2025): 361–72. https://doi.org/10.5281/zenodo.15227194.

Full text
Abstract:
<strong><u>ABSTRACT</u></strong>: Mullerian duct anomalies are rare affecting approximately 1%females with 3% having poor reproductive outcome. These congenital anomalies result due to failure of formation or failure of fusion of the mullerian ducts. According to the American Fertility Society (AFS), the mullerian duct anomalies are classified into seven different categories. Ultrasound is the first imaging investigation in cases of suspected mullerian anomalies while MRI is the key imaging modality of choice due to its capabilities of demonstrating the female genital tract remarkably well and
APA, Harvard, Vancouver, ISO, and other styles
4

Kovarsky, S. L., Yu V. Petrukhina, S. P. Blokh, A. I. Zakharov, and A. A. Bebenina. "Mullerian ducts derivatives in abdominal cryptorchism in children." Andrology and Genital Surgery 22, no. 4 (2021): 77–85. http://dx.doi.org/10.17650/1726-9784-2021-22-4-77-85.

Full text
Abstract:
Disorder of sex determination is a condition associated with clinical and biochemical discrepancy between genetic, gonadal, and phenotypic sex of a child requiring detailed examination for final selection of sex. Indications for sex determination can arise both in infancy and during puberty. Several conditions pertaining to abnormal sex differentiation are manifested as normal male genitalia with Mullerian ducts derivatives.The study objective is to present clinical observations of children with persistent Mullerian duct syndrome.The study presents 2 clinical cases of children with disorders o
APA, Harvard, Vancouver, ISO, and other styles
5

Sawai, Devyani, Susheel Kumar Sharma, Devashish Singh Sawai, Uttkarsha Sawai, Sangeeta Sharma, and Ajay Sharma. "Pregnancy in uterus didelphys delivered by caesarean section: a case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 11 (2017): 5166. http://dx.doi.org/10.18203/2320-1770.ijrcog20175048.

Full text
Abstract:
The aim of this study is to report a rare case of pregnancy in uterus didelphys. Mullerian duct anomalies are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. A didelphys uterus, also known as double uterus is one of the least common amongst the various Mullerian duct anomalies. It results from complete failure of fusion of Mullerian ducts. There is presence of double uterine bodies with two separate cervices and often double or septate vagina. We report the case in our institute of a pregnancy in the left sided body of
APA, Harvard, Vancouver, ISO, and other styles
6

ARA, SARWAT, and TASNEEM ALI. "MULLERIAN DUCT ANOMALIES;." Professional Medical Journal 19, no. 05 (2012): 723–29. http://dx.doi.org/10.29309/tpmj/2012.19.05.2328.

Full text
Abstract:
Background: Müllerian duct anomalies (MDAs) occur with an incidence estimated to be 4.3%. A unicornuate uterus with orwithout a rudimentary horn; is a type of mullerian duct abnormality with a frequency of 0.4%. Rudimentary horn pregnancies are rare obstetriccomplication and may cause difficulty in diagnosis and subsequent management. Objective: To alert about Mullerian duct abnormalitiesespecially unicornuate uterus with or without rudimentary horn. Design: Case series. Setting: Study was conducted in the department ofGynecology and obstetrics unit1, Allied Hospital Faisalabad. Duration of st
APA, Harvard, Vancouver, ISO, and other styles
7

TAHIRA, TASNIM. "MULLERIAN DUCT ANOMALIES." Professional Medical Journal 17, no. 04 (2010): 676–78. http://dx.doi.org/10.29309/tpmj/2010.17.04.3021.

Full text
Abstract:
Aim: The aim of this study was to analyze various presentations of mullerian duct anomalies &amp; to determine its impact on reproductive outcome. Setting: Gynae Unit 1, Allied Hospital, PMC Faisalabad. Period: from 01-06-2007 to 31-12-2008. Design: Case Series Methods: A total of 40 patients were included in study. Their detailed history &amp; examination was done. Relevant investigations TVS, IVU &amp; MRI were done to diagnose mullerian duct malformations. Results: 16 patients (40%) presented with obstructive genital tract malformation while 8 patients (20%) presented with absence of uterus
APA, Harvard, Vancouver, ISO, and other styles
8

Allard, S., P. Adin, L. Gouedard, et al. "Molecular mechanisms of hormone-mediated Mullerian duct regression: involvement of beta-catenin." Development 127, no. 15 (2000): 3349–60. http://dx.doi.org/10.1242/dev.127.15.3349.

Full text
Abstract:
Regression of the Mullerian duct in the male embryo is one unequivocal effect of anti-Mullerian hormone, a glycoprotein secreted by the Sertoli cells of the testis. This hormone induces ductal epithelial regression through a paracrine mechanism originating in periductal mesenchyme. To probe the mechanisms of action of anti-Mullerian hormone, we have studied the sequence of cellular and molecular events involved in duct regression. Studies were performed in male rat embryos and in transgenic mice overexpressing or lacking anti-Mullerian hormone, both in vivo and in vitro. Anti-Mullerian hormone
APA, Harvard, Vancouver, ISO, and other styles
9

Pandya, Manish R., Ghanshyam K. Gorvadiya, and Jeel A. Modesara. "Accessory fallopian tube –A rare anomaly." Indian Journal of Obstetrics and Gynecology Research 10, no. 1 (2023): 88–90. http://dx.doi.org/10.18231/j.ijogr.2023.020.

Full text
Abstract:
Accessory fallopian tube is a rare, congenital and developmental mullerian duct anomaly. The documented incidence is around 6-10% in women seeking for infertility treatment. We observed accessory fallopian tube in a patient during routine checking of operative field, ovaries and fallopian tube during caesarean section. Accessory fallopian tube is congenital anomaly which is attached with ampullary part of main fallopian tube. Accessory fallopian tube is common site for pyosalpinx, hydrosalpinx, cystic swelling and torsion which can lead to infertility and other complications. The ovum released
APA, Harvard, Vancouver, ISO, and other styles
10

Renu, Divya, GaneshB Rao, K. Ranganath, and Namitha. "Persistent mullerian duct syndrome." Indian Journal of Radiology and Imaging 20, no. 1 (2010): 72. http://dx.doi.org/10.4103/0971-3026.59761.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Mullerian duct"

1

Prunskaite-Hyyryläinen, R. (Renata). "Role of Wnt4 signaling in mammalian sex determination, ovariogenesis and female sex duct differentiation." Doctoral thesis, Oulun yliopisto, 2014. http://urn.fi/urn:isbn:9789526204727.

Full text
Abstract:
Abstract Mammalian female sex development was considered a default developmental pathway. However, the deletion of the Wnt4 gene, a member of the Wnt family of secreted signals, was shown to reverse the sex of XX female mouse embryo and caused exhibition of certain male characteristics. This indicated that the female sexual development cannot be default but depends on active signaling and cell-cell interaction. The aim of the current study was to reveal the functional role of the Wnt4 gene in the control of sex determination, ovariogenesis and female sex duct formation. This study demonstrates
APA, Harvard, Vancouver, ISO, and other styles
2

Shy, Hannah Marie. "Mayer-Rokitansky-Kuster-Hauser Syndrome." Thesis, The University of Arizona, 2016. http://hdl.handle.net/10150/612432.

Full text
Abstract:
Mayer-Rokitansky-Kuster-Hauser Syndrome is a congenital disorder of the female reproductive tract due to impaired Müllerian duct development. There are three known categorical presentations: isolated, atypical, and MURCS association. Several developmentally significant factors including inappropriate AMH/AMHR interaction, and mutations in the WNT gene family and HOXA7-13 cluster have been studied. There has also been investigation into an autosomal dominant pattern of inheritance in families with multiple cases of the syndrome. Due to the presence of multiple subsets of patients with similar g
APA, Harvard, Vancouver, ISO, and other styles
3

Bolding, Ellen. "Malignant mixed mullerian tumours of the uterus : an immunohistochemical study." Thesis, University of Cape Town, 1989. http://hdl.handle.net/11427/26270.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Mullerian duct"

1

Al-Salem, Ahmed H., and Moustafa Hamchou. "Persistent Mullerian Duct Syndrome." In Pediatric Gynecology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49984-6_10.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

AbouZeid, Amr Abdelhamid Zaki, and Shaimaa Abdelsattar Mohammad. "Associated Mullerian Duct Anomalies." In Atlas of Anorectal Anomalies. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-10282-0_22.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Arora, Mrinal, and Aparajita Mitra. "Disorders of Anti-Mullerian Hormone and Its Receptors: Persistent Mullerian Duct Syndrome." In Children with Differences in Sex Development. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1639-5_26.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Nistal, Manuel, and Pilar González-Peramato. "Disorders of Sexual Development, Persistent Mullerian Duct Syndrome." In Encyclopedia of Pathology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-28845-1_4801-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Nistal, Manuel, and Pilar González-Peramato. "Disorders of Sexual Development, Persistent Mullerian Duct Syndrome." In Encyclopedia of Pathology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-41894-6_4801.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Buy, Jean Noel, and Michel Ghossain. "Congenital Abnormalities of the Mullerian Ducts." In Gynecological Imaging. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-31012-6_19.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Simpson, Joe Leigh. "Genetics of Female Infertility Due to Anomalies of the Ovary and Mullerian Ducts." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0659-8_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Hinman, Frank, and Laurence S. Baskin. "Excision of Utricular (Mullerian Duct) Cyst." In Hinman's Atlas Of Pediatric Urologic Surgery. Elsevier, 2009. http://dx.doi.org/10.1016/b978-0-7216-0645-3.00175-x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Izhar, Shabnam, Purnima Singh, and Kusum Gupta. "A Case Report on Persistent Mullerian Duct Syndrome." In New Frontiers in Medicine and Medical Research Vol. 12. Book Publisher International (a part of SCIENCEDOMAIN International), 2021. http://dx.doi.org/10.9734/bpi/nfmmr/v12/4099f.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

"Genital anomalies." In Oxford Handbook of Genitourinary Medicine, HIV, and Sexual Health, edited by Laura Mitchell, Bridie Howe, D. Ashley Price, Babiker Elawad, and K. Nathan Sankar. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780198783497.003.0033.

Full text
Abstract:
Genital anomalies considers both congenital and acquired differences in genital anatomy in both men and women. Clinicians performing genital examinations will frequently encounter many of these in their practice, and within this chapter each anomaly is succinctly described and for many the appropriate management is subsequently outlined. In men, the following differences are included: epispadias, hypospadias, lymphocele, paraphimosis, Peyronie’s disease, priapism, phimosis, spermatoceles and epididymal cysts, urethral channels, and varicocele. In women: Bartholin gland pathology (cysts and abs
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Mullerian duct"

1

Josephine, Arpitha, and Dhanush Jayanna. "Mullerian duct anomalies: the hidden roadblocks to reproduction." In Radiopaedia 2025 Virtual Conference. Radiopaedia.org, 2025. https://doi.org/10.53347/rposter-3140.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Gaboardi, Franco, Andrea Bozzola, Tiziano Zago, Gildo M. Gulfi, and Luigi Galli. "Recanalization of azoospermia due to a Mullerian duct cyst by Nd:YAG laser." In Optics, Electro-Optics, and Laser Applications in Science and Engineering, edited by Graham M. Watson, Rudolf W. Steiner, and Joseph J. Pietrafitta. SPIE, 1991. http://dx.doi.org/10.1117/12.43911.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Ghammem, Nour, Ines Lasmar, Hajer Ben Mansour, Fadoua Bouguerra, Ghada Abdessatar, and Amel Mezlini. "#211 A rare case of persistent mullerian duct syndrome with testicular seminoma." In ESGO 2023 Congress. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/ijgc-2023-esgo.239.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Saleh Al Mousa, Shaden, Nufe Al Mansor, Ammar Ashraf, et al. "14 Testicular seminoma in an infertile adult patient with persistent mullerian duct syndrome." In Abstracts from the Fellowship of Postgraduate Medicine Centenary Conference 2018: Transforming Health and Health Care. The Fellowship of Postgraduate Medicine, 2018. http://dx.doi.org/10.1136/postgradmedj-2018-fpm.25.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Soni, Abhishek, Nupur Bansal, A. K. Dhull, Vivek Kaushal, Rajeev Atri, and Monica Verma. "Diagnostic dilemma of mesonephric adenocarcinoma cervix." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685283.

Full text
Abstract:
Introduction: Mesonephric carcinoma is a rare type of epithelial tumor of the uterine cervix which derive from the remnants of the paired mesonephric (Wolff’s) ducts. The incidence of such neoplasms is difficult to determine due to rarity, previous misclassification of clear cell carcinomas and yolk sac tumours as mesonephric carcinomas and potential underreporting due to misclassification of mesonephric carcinoma as Mullerian tumours or mesonephric hyperplasia. The evidence regarding the clinical course, prognosis and optimal treatment is limited. Materials and Methods: Searches were performe
APA, Harvard, Vancouver, ISO, and other styles
6

Liu, Ying, Elena Enbom, Hai-Yun Yen, Robert Maxson, and Louis Dubeau. "Abstract 3262: Role of the mullerian ducts in the development of genito-urinary organs and coelomic epithelial tissues in female mice." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-3262.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Mullerian duct' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography