The ESHRE/ESGE Consensus on the Classification of Female Genital Tract
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Genetic Syndromes and Genes Involved
ndrom Sy es tic & e G n e e n G e f Connell et al., J Genet Syndr Gene Ther 2013, 4:2 T o Journal of Genetic Syndromes h l e a r n a DOI: 10.4172/2157-7412.1000127 r p u y o J & Gene Therapy ISSN: 2157-7412 Review Article Open Access Genetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene Therapy Connell MT1, Owen CM2 and Segars JH3* 1Department of Obstetrics and Gynecology, Truman Medical Center, Kansas City, Missouri 2Department of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 3Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA Abstract Müllerian and vaginal anomalies are congenital malformations of the female reproductive tract resulting from alterations in the normal developmental pathway of the uterus, cervix, fallopian tubes, and vagina. The most common of the Müllerian anomalies affect the uterus and may adversely impact reproductive outcomes highlighting the importance of gaining understanding of the genetic mechanisms that govern normal and abnormal development of the female reproductive tract. Modern molecular genetics with study of knock out animal models as well as several genetic syndromes featuring abnormalities of the female reproductive tract have identified candidate genes significant to this developmental pathway. Further emphasizing the importance of understanding female reproductive tract development, recent evidence has demonstrated expression of embryologically significant genes in the endometrium of adult mice and humans. This recent work suggests that these genes not only play a role in the proper structural development of the female reproductive tract but also may persist in adults to regulate proper function of the endometrium of the uterus. -
Reproductive Outcomes After Hysteroscopic Metroplasty for Women with Dysmorphic Uterus and Recurrent Implantation Failure
Original paper Reproductive outcomes after hysteroscopic metroplasty for women with dysmorphic uterus and recurrent implantation failure J. FERRO1, E. LABARTA2, C. SANZ3, P. MONTOYA3, J. REMOHI4 1Director of Surgery of Instituito Valenciano de Infertilidad “IVI”, Plaza de la Policía Local, 3. 46015. Valencia, Spain; 2 Especialist in Reproductive Medicine of Instituito Valenciano de Infertilidad “IVI”; 3Fellows in Reproductive Medicine of Instituito Valenciano de Infertilidad “IVI”. 4Director of Instituto Valenciano de Infertilidad “IVI. Correspondence at: Jaime Ferro, Instituito Valenciano de Infertilidad “IVI”, Plaza de la Policía Local, 3. 46015. Valencia, Spain; e-mail: [email protected] Abstract Background: The aim of this study was to assess the reproductive outcomes of women with recurrent implantation failure (RIF) after hysteroscopic metroplasty for dysmorphic uteri. Methods: This retrospective observational study included 190 women with a diagnosis of RIF. These patients were eligible for hysteroscopic metroplasty for dysmorphic uteri, including T-shaped uteri, between January 2008 and September 2015 at the Instituto Valenciano de Infertilidad (IVI) in Valencia, Spain. Results: The total clinical pregnancy rate, the live birth rate, and the abortion rate were 80.0% (152/190), 77.9% (147/190) and 8.9%, respectively. At 12 months, the clinical pregnancy rate was 76.3% (145/190) and at 6 months 50.5% (96/190). After the metroplasty, approximately 76% of all gravidities, were achieved during the first 12 months of follow-up. Within the first IVF cycle, pregnancy and live birth rates were 77.8% and 86.1%, respectively. The mean time to pregnancy was 6.5 months. Conclusions: This study demonstrates that hysteroscopic metroplasty improves pregnancy and live birth rates for women with a history of recurrent implantation failure and dysmorphic uterus. -
Prevalence of Mullerian Anomaly Among Infertile Patients
European Journal of Molecular & Clinical Medicine (EJMCM) ISSN: 2515-8260 Volume 07, Issue 10, 2020 Original research article Prevalence of Mullerian Anomaly among infertile patients Dr Swet Nisha1, Dr Kalpana Singh2, Dr Shubhanti Kumari3 1 Senior Resident, Department of Reproductive Medicine, IGIMS, Patna, Bihar, India 2 Additional Professor, Department of Reproductive Medicine, IGIMS, Patna, Bihar, India 3 Assistant Professor, Department of Reproductive Medicine, IGIMS, Patna, Bihar, India Corresponding Author: Dr Kalpana Singh Abstract Background: To evaluate the prevalence of Müllerian anomalies (MAs) among infertile women came for fertility treatments (intrauterine insemination or IVF (In vitro fertilization) cycles. Aim: To calculate the prevalence of mullerian anomaly and each subtype among infertile women. Methods: This is a retrospective observational study based upon a cohort of infertile women, who underwent hysteroscopy and laparoscopy as part of the basic infertility workup from 2018 to 2019, at department of Reproductive Medicine in IGIMS, Patna. Results: A total of 160 women were included in the study. The prevalence of mullerian anomaly was 8.13% (n=13). The prevalence of different subtypes among women with mullerian anomaly were: septate uterus 53.85% (n = 7), arcuate uterus 23.08% (n = 3), bicornuate uterus 7.69% (n = 1), unicornuate uterus 7.69 % (n = 1) and didelphys uterus 7.69% (n = 1). We did not find any case of uterine hypoplasia/agenesis or unclassified type. Women with mullerian anomaly who achieved pregnancy were: 38.46% (n = 5). Highest pregnancy rate was associated with septate uterus after hysteroscopic correction, at 42.86% (3/7). Conclusions: The prevalence of mullerian anomaly among infertile women may be considered as low. -
Vaginal Agenesis: a Case Report*
Vaginal agenesis: A case report* By Reyalu T. Tan, MD; Sigrid A. Barinaga, MD, FPOGS; and Marie Janice S. Alcantara, MD, FPOGS Department of Obstetrics and Gynecology, Southern Philippine Medical Center ABSTRACT Congenital anomalies of the vagina are rare congenital anomalies. Women born with this anomaly present with collection of blood in the uterine cavity or hematometra and pelvic pain. Presented is a case of a 12-year old girl with hypogastric pain and primary amenorrhea complicated by vaginal agenesis. She was managed conservatively by creating a neovagina with the use of bipudendal flap or Modified Singapore flap. Management can be non-surgical or surgical but the management of congenital vaginal agenesis remains controversial. The decision to do a conservative surgical procedure or a hysterectomy depends on the clinical profile of the patient, the expertise of the surgeons, the extent of the anomaly, and its association to other congenital anomalies. Keywords: Vaginal Agenesis, Hematometra, Primary Amenorrhea, Modified Singapore flap INTRODUCTION congenital anomaly. The patient is an Elementary student, non-smoker, non-alcoholic beverage drinker, 2nd child of a evelopmental anomalies in mullerian ducts and G5P5 mother. urogenital sinus represent some of the most Two months prior to admission, the patient had Dinteresting disorders in Obstetrics and Gynecology. sudden onset of severe abdominal pain. Admitted at Normal development of the female reproductive system a local hospital and managed as a case of Ovarian New leads to differentiation of the reproductive structures. Growth with complication. At laparotomy, the patient Vaginal agenesis is the congenital absence of vagina was noted with hemoperitoneum (100 milliliter) with where there is failure of formation of the sinovaginal bulb the left fallopian tube enlarged to 5 x 9 centimeter with a which leads to outflow tract obstruction and infertility. -
Congenital Uterine Anomalies: the Role of Surgery Maria Carolina Fernandes Lamouroux Barroso M 2021
MESTRADO INTEGRADO EM MEDICINA Congenital uterine anomalies: the role of surgery Maria Carolina Fernandes Lamouroux Barroso M 2021 Congenital uterine anomalies: the role of surgery Dissertação de candidatura ao grau de Mestre em Medicina, submetida ao Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto Maria Carolina Fernandes Lamouroux Barroso Aluna do 6º ano profissionalizante de Mestrado Integrado em Medicina Afiliação: Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto Endereço: Rua de Jorge Viterbo Ferreira nº228, 4050-313 Porto Endereço eletrónico: [email protected]; [email protected] Orientador: Dra. Márcia Sofia Alves Caxide e Abreu Barreiro Diretora do Centro de Procriação Medicamente Assistida e do Banco Público de Gâmetas do Centro Materno-Infantil do Norte Assistente convidada, Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto. Afiliação: Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto Endereço: Largo da Maternidade de Júlio Dinis 45, 4050-651 Porto Endereço eletrónico: [email protected] Coorientador: Prof. Doutor Hélder Ferreira Coordenador da Unidade de Cirurgia Minimamente Invasiva e Endometriose do Centro Materno- Infantil do Norte Professor associado convidado, Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto. Afiliação: Instituto de Ciências Biomédicas Abel Salazar – Universidade do Porto Endereço: Rua Júlio Dinis 230, B-2, 9º Esq, Porto Endereço eletrónico: [email protected] Junho 2021 Porto, junho de 2021 ____________________________________ (Assinatura da estudante) ____________________________________ (Assinatura da orientadora) ____________________________________ (Assinatura do coorientador) ACKNOWLEDGEMENTS À Dra. Márcia Barreiro, ao Dr. Luís Castro e ao Prof. Doutor Hélder Ferreira, por toda a disponibilidade e empenho dedicado à realização deste trabalho. Aos meus pais, irmão e avós, pela participação que desde sempre tiveram na minha formação, e pelo carinho e apoio incondicional. -
Vaginal Reconstruction for Distal Vaginal Atresia Without Anorectal Malformation: Is the Approach Diferent?
Pediatric Surgery International (2019) 35:963–966 https://doi.org/10.1007/s00383-019-04512-2 ORIGINAL ARTICLE Vaginal reconstruction for distal vaginal atresia without anorectal malformation: is the approach diferent? Andrea Bischof1 · Veronica I. Alaniz2 · Andrew Trecartin1 · Alberto Peña1 Accepted: 20 June 2019 / Published online: 29 June 2019 © Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract Introduction Distal vaginal atresia is a rare condition and treatment approaches are varied, usually driven by symptoms. Methods A retrospective review was performed to identify patients with distal vaginal atresia without anorectal malforma- tion. Data collected included age and symptoms at presentation, type and number of operations, and associated anomalies. Results Eight patients were identifed. Four presented at birth with a hydrocolpos and four presented with hematomet- rocolpos after 12 years of age. Number of operations per patient ranged from one to seven with an average of three. The vaginal reconstruction was achieved by perineal vaginal mobilization in four patients and abdomino-perineal approach in four patients. One patient, with a proximal vagina approximately 7 cm from the perineum, required partial vaginal replace- ment with colon. In addition, she had hematometrocolpos with an acute infammation at the time of reconstruction despite menstrual suppression and drainage which may have contributed to the difculty in mobilizing the vagina. In fve patients, distal vaginal atresia was an isolated anomaly. In the other three cases, associated anomalies included: mild hydronephrosis that improved after hydrocolpos decompression (2), cardiac anomaly (2), and vertebral anomaly (1). Conclusion In this series, a distended upper vagina/uterus was a common presentation and the time of reconstruction was driven by the presence of symptoms. -
Elixir Journal
45637 Ganesh Elumalai and Jenefa Princess / Elixir Embryology 103 (2017) 45637-45640 Available online at www.elixirpublishers.com (Elixir International Journal) Embryology Elixir Embryology 103 (2017) 45637-45640 “CLOACAL MEMBRANE ANOMALIES” EMBRYOLOGICAL BASIS AND ITS CLINICAL IMPORTANCE Ganesh Elumalai and Jenefa Princess Department of Embryology, College of Medicine, Texila American University, South America. ARTICLE INFO ABSTRACT Article history: Cloacal malformation is a rare but important anomaly. The cloacal anomaly is Received: 1 January 2017; characterised by the persistence of a common channel draining the urinary, genital and Received in revised form: alimentary tracts through a single orifice. It results from abnormal compartmentalization 1 February 2017; of features that are normal in the primitive female embryo. Abnormal embryology and Accepted: 10 February 2017; cloacal anatomy are described in detail. Cloacal abnormalities are usually diagnosed promptly in the neonatal period. Keywords © 2017 Elixir All rights reserved. Cloacal membrane, Uro-rectal septum, Extrophy of the cloaca, Recto-urinary fistulas, Anal agenesis, Rectal atresia. Introduction dilate them to make an anus.. Initial management focuses on Abnormal cloacal development takes place when rectum, anatomic remodelling of the urinary and gastrointestinal vagina and lower urinary tract fuse into a single common system to achieve continence. Improved paediatric channel. Persistent cloaca is a most severe malformation of management strategies have increased the patient survival into cloacal anomalies in girls and is associated with complex adult life. In order to provide appropriate advice, clinicians pelvic malformations. The abnormality of these structures who are undertaking life-long management of adolescent and varies from bladder neck to just beneath the perineal skin. -
Congenital Uterine Anomalies in Women with Recurrent Miscarriage
promoting access to White Rose research papers Universities of Leeds, Sheffield and York http://eprints.whiterose.ac.uk/ This is an author produced version of a paper published in Human Reproduction Update. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/9074/ Published paper Saravelos, S.H., Cocksedge, K.A. and Li, T-C. (2008) Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal. Human Reproduction Update, 14 (5). pp. 415-429. http://dx.doi.org/10.1093/humupd/dmn018 White Rose Research Online [email protected] Saravelos et al. Human Reproduction Update 2008 14(5):415-429 TITLE Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: A critical appraisal RUNNING TITLE Congenital uterine anomalies in reproductive failure AUTHORS Sotirios H Saravelos1, 3, Karen A. Cocksedge1, Tin-Chiu Li1, 2 ADDRESS 1 Reproductive Medicine and Surgery Unit, University of Sheffield, Sheffield Teaching Hospitals, Jessop Wing, Tree Root Walk, Sheffield, S10 2SF, UK. 2 Biomedical Research Unit, Jessop Wing, Tree Root Walk, Sheffield, S10 2SF, UK 3 To whom correspondence should be addressed: Email [email protected] Saravelos et al. Human Reproduction Update 2008 14(5):415-429 ABSTRACT BACKGROUND: The prevalence of congenital uterine anomalies in women with reproductive failure remains unclear, largely due to methodological bias. The aim of this review is to assess the diagnostic accuracy of different methodologies and estimate the prevalence of congenital uterine anomalies in women with infertility and recurrent miscarriage (RM). METHODS: Studies from 1950-2007 were identified through a computer MEDLINE search; all relevant references were further reviewed. -
1- Development of Female Genital System
Development of female genital systems Reproductive block …………………………………………………………………. Objectives : ✓ Describe the development of gonads (indifferent& different stages) ✓ Describe the development of the female gonad (ovary). ✓ Describe the development of the internal genital organs (uterine tubes, uterus & vagina). ✓ Describe the development of the external genitalia. ✓ List the main congenital anomalies. Resources : ✓ 435 embryology (males & females) lectures. ✓ BRS embryology Book. ✓ The Developing Human Clinically Oriented Embryology book. Color Index: ✓ EXTRA ✓ Important ✓ Day, Week, Month Team leaders : Afnan AlMalki & Helmi M AlSwerki. Helpful video Focus on female genital system INTRODUCTION Sex Determination - Chromosomal and genetic sex is established at fertilization and depends upon the presence of Y or X chromosome of the sperm. - Development of female phenotype requires two X chromosomes. - The type of sex chromosomes complex established at fertilization determine the type of gonad differentiated from the indifferent gonad - The Y chromosome has testis determining factor (TDF) testis determining factor. One of the important result of fertilization is sex determination. - The primary female sexual differentiation is determined by the presence of the X chromosome , and the absence of Y chromosome and does not depend on hormonal effect. - The type of gonad determines the type of sexual differentiation in the Sexual Ducts and External Genitalia. - The Female reproductive system development comprises of : Gonad (Ovary) , Genital Ducts ( Both male and female embryo have two pair of genital ducts , They do not depend on ovaries or hormones ) and External genitalia. DEVELOPMENT OF THE GONADS (ovaries) - Is Derived From Three Sources (Male Slides) 1. Mesothelium 2. Mesenchyme 3. Primordial Germ cells (mesodermal epithelium ) lining underlying embryonic appear among the Endodermal the posterior abdominal wall connective tissue cell s in the wall of the yolk sac). -
Ectopic Pregnancy in a Case of Congenital Mullerian Anomaly: a Diagnostic Dilemma
International Journal of Reproduction, Contraception, Obstetrics and Gynecology Brahmbhatt S et al. Int J Reprod Contracept Obstet Gynecol. 2020 Aug;9(8):3512-3514 www.ijrcog.org pISSN 2320-1770 | eISSN 2320-1789 DOI: http://dx.doi.org/10.18203/2320-1770.ijrcog20203354 Case Report Ectopic pregnancy in a case of congenital mullerian anomaly: a diagnostic dilemma Sanjay Brahmbhatt1, Amrita Makhija2, Jayna Brahmbhatt1, Yagnesh V. Patel1* 1Department of Gynecological Endoscopy, Himalaya Hospital, Anand, Gujarat, India 2Department of Obstetrics and Gynecology, Himalayan Institute of Medical Sciences, Dehradun, Uttarakhand, India Received: 22 May 2020 Accepted: 30 June 2020 *Correspondence: Dr. Yagnesh V. Patel, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Ectopic or extrauterine pregnancy occurring in a case with mullerian defect is very rare and poses diagnostic challenges. Undescended and non-communicating fallopian tubes are extremely rare mullerian anomalies. Here authors present a case of ectopic pregnancy occurring in an undescended non-communicating fallopian tube in a patient with unicornuate uterus with absent horn, which was managed laparoscopically. A 32-year-old lady, diagnosed case of left unicornuate uterus with absent right horn, was referred to us with the suspicion of ruptured ectopic pregnancy. The abdominopelvic ultrasound showed a soft tissue lesion of size 32×24 mm, towards the right lateral pelvic wall near the iliac vessels, with increased vascularity on colour flow doppler. -
Anomalies Utérines Et Vaginales Transversales: Données De Génétique Du Développement Et Apport Personnel Sur L'étude D
Anomalies utérines et vaginales transversales: données de génétique du développement et apport personnel sur l’étude du syndrome de Mayer-Rokitansky-Kuster Séverine Veyrières To cite this version: Séverine Veyrières. Anomalies utérines et vaginales transversales: données de génétique du développe- ment et apport personnel sur l’étude du syndrome de Mayer-Rokitansky-Kuster. Sciences du Vivant [q-bio]. 2000. hal-01733963 HAL Id: hal-01733963 https://hal.univ-lorraine.fr/hal-01733963 Submitted on 14 Mar 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. AVERTISSEMENT Ce document est le fruit d'un long travail approuvé par le jury de soutenance et mis à disposition de l'ensemble de la communauté universitaire élargie. Il est soumis à la propriété intellectuelle de l'auteur. Ceci implique une obligation de citation et de référencement lors de l’utilisation de ce document. D'autre part, toute contrefaçon, plagiat, reproduction illicite encourt une poursuite pénale. Contact : [email protected] LIENS Code de la Propriété Intellectuelle. -
Diagnosis and Treatment of Prenatal Urogenital Anomalies: Review Of
Review Article iMedPub Journals Translational Biomedicine 2015 http://www.imedpub.com ISSN 2172-0479 Vol. 6 No. 3:24 DOI: 10.21767/2172-0479.100024 Diagnosis and Treatment of Prenatal Gautam Dagur1, Kelly Warren1, Urogenital Anomalies: Review of Current Reese Imhof1, Literature Robert Wasnick2 and Sardar A Khan1,2 1 Department of Physiology and Abstract Biophysics, SUNY at Stony Brook, New York 11794, USA With current advances in antenatal medicine it is feasible to diagnose prenatal anomalies earlier and potentially treat these anomalies before they become 2 Department of Urology, SUNY at Stony a significant postnatal problem. We discuss different methods and signs of Brook, New York 11794, USA urogenital anomalies and emphasize the use of telemedicine to assist patients and healthcare providers in remote healthcare facilities, in real time. We discuss prenatal urogenital anomalies that can be detected by antenatal ultrasound and Corresponding author: Sardar Ali Khan fetal magnetic resonance imaging. Ultimately, we address the natural history of urogenital anomalies, which need surgical intervention, and emphasize ex-utero intrapartum treatment procedures and other common surgical techniques, which [email protected] alter the natural history of urogenital anomalies. Keywords: Prenatal anomalies; Hydronephrosis; Kidney; Ureter; Bladder; Urethra; Professor of Urology and Physiology, HSC Level 9 Room 040 SUNY at Stony Brook, Oligohydraminos; Genitourinary Stony Brook, NY 11794-8093,USA. Abbreviations: US: Ultrasound; GU: Genitourinary;