41. Birth Disorder Information Directory - V (Von mayer) rokitansky kuster (hauser) syndrome (MRK Anomaly; Uterus BipartitusSolidus Rudimentarius Cum Vagina Solida; Vaginal Atresia; Vagina, http://www.bdid.com/defectv.htm

HOME V VACTERL Association (VATER Association) List of Sites with Hydrocephalus See Sujansky Leonard Syndrome Vaginal Agenesis See Mayer Rokitansky Kuster Hauser Syndrome Vagneur Triolle Ripert Syndrome Vagneur triolle ripert syndrome Valproic Acid Antenatal Infection See Fetal Valproic Syndrome Van Allen Myhre Syndrome Van allen myhre syndrome Van Bervliet Syndrome (Arthrogryposis IUGR Thoracic Dystrophy) Van bervliet syndrome Van Biervliet Hendrickx van Ertbruggen Syndrome (Craniofacial Dysostosis Arthrogryposis Progeroid Appearance) Craniofacial dysostosis arthrogryposis progeroid appearance Van Bogaert Hozay Syndrome VAN BOGAERT-HOZAY SYNDROME Van Buchem Disease (Endosteal Hyperostosis, Hyperostosis Corticalis Generalisata, Hyperphosphatasemia Tarda) HYPEROSTOSIS CORTICALIS GENERALISATA Van de Berghe Dequeker Syndrome (Ulnar Hypoplasia Lobster Claw Deformity of Feet) Van de berghe dequeker syndrome ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET Van den Bosch Syndrome Van den bosch syndrome VAN DEN BOSCH SYNDROME Van den Ende Brunner Syndrome (Ectrodactyly with Cardiopathy and Dysmorphism) ectrodactyly cardiopathy dysmorphism Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome See Waardenburg (Klein) Syndrome Van der Woude Syndrome (Cleft Lip and/or Palate, Mucous Cysts of Lower Lip, Lip Lit Syndrome)

42. Vaginal Atresia RKH syndrome VON mayer rokitansky - kuster ANOMALY MRK ANOMALY See vagina,absence of ( rokitansky - kuster - hauser syndrome; 277000 ) mayer http://ibis-birthdefects.org/start/vaginal.htm

Tips for printing Vaginal Atresia About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and ROKITANSKI - KUSTER - HAUSER SYNDROME RKH SYNDROME VON MAYER - ROKITANSKY - KUSTER ANOMALY MRK ANOMALY UTERUS BIPARTITUS SOLIDUR RUDIMENTARIUS COM VAGINA SOLIDA Special Resources Vaginal Atresia A Selection of Internet Sites [*] Outstanding [P] Professional [Dutch] [Spanish] VAGINA, ABSENCE OF VAGINAL ATRESIA ROKITANSKI - KUSTER - HAUSER SYNDROME; RKH SYNDROME; VON MAYER - ROKITANSKY - KUSTER ANOMALY; MRK ANOMALY; UTERUS BIPARTITUS SOLIDUR RUDIMENTARIUS COM VAGINA SOLIDA; by OMIM In addition to congenital absence of the vagina, are normal female secondary sexual characteristics, rudimentary uterus in the form of bilateral and noncanaliculated msucular buds, normal tubes and ovaries and normal endocrine and cytogenetic evaluations ... [*] [P] MULLERIAN APLASIA by OMIM Shokeir (1978) described 28 unrelated females, aged 15 to 28, with aplasia of the mullerian duct derivatives. Their complaints were amenorrhea and difficulty or pain on attempting sexual intercourse; absence of the vagina and failure to palpate the uterus rectally were features in all ... The pedigree pattern was consistent with female - limited autosomal dominant inheritance. The disorder was transmitted through normal males. See vagina, absence of ( Rokitansky - Kuster - Hauser syndrome; 277000 ) ...

43. MRKH - Mayer-Rokitansky-Küster-Hauser Syndrome Välkommen till min sida om mayerrokitansky-kuster-hauser syndrom, även kallatvaginal- och livmoderagenesis! http://biphome.spray.se/torahr/

Välkommen till min sida som handlar om ett intersexsyndrom som förtjänar lite mer uppmärksamhet Presentation Beskrivning Historia Behandling ... Länkar Mayer-Rokitansky-Küster-Hauser Syndrome Kallas även för Müllersk agenesis, vaginal- och livmoderagenesis /-aplasi H är har jag samlat lite information om ett intersexsyndrom som inte är särskilt känt. MRKH är relativt ovanligt och återfinns hos ca 1 av 5 000 kvinnor. Syndromet innebär att man saknar livmoder och vagina. Presentation Beskrivning Identitet Historia ... Texter M R K H Syndrome Maila Till Mig

44. Laparoscopic Rectosigmoid Colpopoiesis As Treatment For A Patient of the vagina is known as mayerrokitansky-kuster-hauser (MRKH) syndrome. Then she was diagnosed as having mayer-rokitansky-kuster-hauser syndrom. http://www.cmj.org/information/full.asp?id=528

45. Laparoscopic Rectosigmoid Colpopoiesis As Treatment For A Patient Laparoscopic rectosigmoid colpopoiesis as treatment for a patient with mayerrokitansky-kuster-hauser syndrome. WAN Xiaoping ?, XI Xiaowei ?, http://www.cmj.org/information/abstract.asp?id=528

46. Teen Growth, The Teen Resource For Advice, Health Information, Social Interactio I have mayerrokitansky-kuster-hauser syndrome/Muellerian aplasia. What is thedifference is between MRKH and Muellerian aplasia. Are there other resources http://www.teengrowth.com/index.cfm?action=info_advice&ID_Advice=2447&category=h

47. PATIENT PLATFORM Vaginal agenesis (mayer rokitansky - kuster - hauser syndrome) recentetiopathogenetical and anatomical views. Clin Exp Obstet Gynecol 9, 98-102 (1982) http://www.bioscience.org/patient/rokitans.htm

FRONTIERS IN BIOSCIENCE; PATIENT PLATFORM Each question will be responded to after the subject has been carefully investigated. However, Frontiers in Bioscience merely provides the information as a general guide to help patients and with the understanding that the contributors can not accept any type of liability for the use of the information. The information can not substitute expert medical advice and should be regarded as the starting point for finding the proper medial treatment. Questions are subject to editorial corrections. Question: I am seeking information regarding the treatment and postoperative management of Rokitansky syndrome. My 17 year-old daughter was recently diagnosed with this disorder, and we need help deciding what the treatment options, and the postoperative outcome may be. References from Medline MEDLINE reports MEDLINE abstracts MEDLARS reports ASN.1 reports MEDLINE neighbors protein links nucleotide links structure links genome links Back into Entrez for All Selected articles below. van Bever, 1992

48. The Journal Of Urology - UserLogin Vaginal atresia in patients with mayerrokitansky-kuster-hauser syndrome is causedby aplasia of the müllerian ducts. The anomaly has various presentations. http://www.jurology.com/pt/re/juro/fulltext.00005392-200309000-00040.htm

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49. The Journal Of Urology - Fulltext: Volume 162(3-II) September 1999 P 1138-1139 T The mayerrokitansky-kuster-hauser syndrome is caused by mullerian aplasia, witha spectrum of abnormalities, including a normal vulva, the presence of a http://www.jurology.com/pt/re/juro/fulltext.00005392-199909000-00061.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive TREATMENT OF THE MAYER-ROKITANSKY-KUSTER-HAUSER... ARTICLE LINKS: Abstract PDF (33 K) References (9) View full size inline images The Journal of Urology Volume 162(3-II) September 1999 pp 1138-1139 TREATMENT OF THE MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME IN BANGLADESH: RESULTS OF 10 TOTAL VAGINAL REPLACEMENTS WITH SIGMOID COLON AT A MISSIONARY HOSPITAL DEL ROSSI, CARMINE; ATTANASIO, ANNA; DOMENICHELLI, VINCENZO; DE CASTRO, ROBERTO From Saint Mary's Sick Assistance Center, Khulna, Bangladesh, and Division of Pediatric Surgery, Azienda Ospedaliera, Parma, European Institute of Oncology, Milan and Department of Pediatric Surgery, Bologna University Medical School, Bologna, Italy Article Outline Abstract MATERIALS AND METHODS RESULTS DISCUSSION ... Citing Articles Figures/Tables Table 1 Abstract TOP Purpose: We report our experience with treating the Mayer-Rokitansky-Kuster-Hauser syndrome in a developing country. The operations were performed by a pediatric surgical team at a missionary hospital in Khulna, Bangladesh. Materials and Methods : From 1995 to 1998, 10 young women with the Mayer-Rokitansky-Kuster-Hauser syndrome underwent complete vaginal replacement. In 4 patients the abnormality was discovered after marriage at the initial sexual approach and, thus, the husband abandoned 3. In 4 of the 10 cases the diagnosis was suspected because of absent menstruation. A physician made the diagnosis in only 2 cases. Preoperatively abdominal ultrasound in 3 patients showed a hypoplastic uterus in all and a right solitary pelvic kidney in 1. In all 10 women a neovagina was created using a 14 cm. segment of sigmoid colon. Two weeks postoperatively patients were taught to dilate and irrigate the neovagina.

50. Journal Of Pelvic Medicine & Surgery - UserLogin mayerrokitansky-kuster-hauser syndrome Presenting as an Inguinal Mass and Herniain the Female Patient. Bidus, Michael A. MD, LCDR, MC, USNR*; Martin, http://www.jpelvicsurgery.com/pt/re/spv/fulltext.00146866-200407000-00002.htm

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51. Journal Of Pelvic Medicine & Surgery - Abstract: Volume 10(4) July/August 2004 P mayerrokitansky-kuster-hauser syndrome Presenting as an Inguinal Mass and Herniain the Female Patient. Journal of Pelvic Medicine Surgery. http://www.jpelvicsurgery.com/pt/re/spv/abstract.00146866-200407000-00002.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive Mayer-Rokitansky-Kuster-Hauser... ARTICLE LINKS: Fulltext PDF (136 K) Mayer-Rokitansky-Kuster-Hauser Syndrome Presenting as an Inguinal Mass and Hernia in the Female Patient. Bidus, Michael A. MD, LCDR, MC, USNR *; Martin, James N. Jr MD +; Magann, Everett F. MD, CAPT, Mc, USNR-R ++ Abstract: Objectives: Complete mullerian agenesis is the second most common condition usually diagnosed during a work-up for primary amenorrhea. A detailed gynecologic history and pelvic examination are the foundations for establishing the diagnosis. Methods: An 18-year-old nulligravida presented to the General Surgery Service complaining of right-sided lower abdominal pain. Upon dissection of the right inguinal canal, it was noted that the hernia sac contained the right ovary and fallopian tube. An intraoperative consult to the Gynecology Service was obtained. The hernia was reduced and the ovary returned to the pelvis. Pelvic examination under anesthesia revealed a severely shortened vagina. A diagnostic laparoscopy was performed revealing complete mullerian agenesis. Postoperative evaluation included a normal karyotype and normal intravenous pyelogram (IVP). Results: The differential diagnosis of inguinal masses in women should include mullerian tract abnormalities.

52. Indigopedia:MRKH - IndigoWiki MRKH An acronym for mayerrokitansky-kuster-hauser syndrome, a relativelyrare (15000 female births) condition marked by primary Amenorrhoea, http://wolfandturtle.net/Indigo/index.php/Indigopedia:MRKH

Indigopedia:MRKH From IndigoWiki MRKH An acronym for M ayer- R okitansky- K uster- H auser syndrome, a relatively rare (1:5,000 female births) condition marked by primary Amenorrhoea , an absent or immature vagina, an absent or immature uterus, and the presence of functional ovaries and a normal 46XX Karyotype Sometimes referred to as Mullerian Agenesis, Vaginal Agenesis, Congenital Absence of Vagina. edit Navigation Back to Main Page Back to Indigopedia Retrieved from " http://wolfandturtle.net/Indigo/index.php/Indigopedia:MRKH Categories Indigopedia Views Article Discussion Edit History Personal tools Create an account or log in Navigation Main Page Community Site News Recent changes ... Help Search Toolbox What links here Related changes Upload file Special pages ... Printable version This page has been accessed 149 times. This page was last modified 20:01, 1 February 2005 by Myria About IndigoWiki

53. IngentaConnect Laparoscopic Creation Of A Neovagina In Mayer-Rokitansky-Kuster-H Laparoscopic Creation of a Neovagina in mayerrokitansky-kuster-hauser syndrome aplasia in three patients with mayer-rokitansky-kuster-hauser syndrome. http://www.ingentaconnect.com/content/aagl/jaagl/2001/00000008/00000003/art00018

Home About Ingenta Ingenta Labs Help For Publishers Why go online? Why choose IngentaConnect? Why choose CustomConnect? Access and authentication ... Contact us For Researchers About IngentaConnect Search and browse Publications available Accessing articles ... Register For Librarians Why choose IngentaConnect? Why choose IngentaConnect Premium? Activating Subscriptions Purchasing articles ... Browse Publications Authors: Marwah V.; Bhandari S.K. Source: The Journal of the American Association of Gynecologic Laparoscopists , Volume 8, Number 3, 1 August 2001, pp. 416-424(9) Publisher: American Association of Gynaecological Laparoscopists View Table of Contents full text options Abstract: Document Type: Original article The full text article is available for purchase $30.00 plus tax The exact price (including tax) will be displayed in your shopping cart before you check out. You will be able to remove this item from your shopping cart at any time before you have completed check-out. View Table of Contents Back to top Terms and Conditions Page Help Quick Search Electronic content Fax/Ariel content Journal or book title Sign in: User name Password Remember me forgotten your password?

54. Mayer - Rokitansky Syndrome And Anorectal Malformation Patankar Shreeprasad P, K mayer rokitansky kuster Houser syndrome (MRKH syndrome) is characterized by Mullerian mayerrokitansky-Küster-hauser syndrome More Details (MRKH) is http://www.ijppediatricsindia.org/article.asp?issn=0019-5456;year=2004;volume=71

55. 277000 VAGINA, ABSENCE OF VAGINAL ATRESIA rokitanskykuster-hauser syndrome RKH syndrome VON mayer-rokitansky-kusterANOMALY mayer-rokitansky-kuster-hauser syndrome MRK ANOMALY http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:277000] -e

56. Journal Of Computer Assisted Tomography - Abstract: Volume 22(5) September/Octob Tumor in Ectopic Omental Ovary in mayerrokitansky-kuster-hauser syndrome CTFindings. Journal of Computer Assisted Tomography. 22(5)758-759, http://www.jcat.org/pt/re/jcat/abstract.00004728-199809000-00018.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive Tumor in Ectopic Omental Ovary... ARTICLE LINKS: Fulltext Permissions Tumor in Ectopic Omental Ovary in Mayer-Rokitansky-Kuster-Hauser Syndrome: CT Findings. Journal of Computer Assisted Tomography. 22(5):758-759, September/October 1998. Rodriguez, Esther; Pombo, Francisco; Alvarez, Carlos; Arnal, Francisco Subscribe to RSS feed utrdc-pt02 Release 4.0

57. Hum. Reprod. -- Sign In Page mayer–von rokitansky–Küster–hauser syndrome (MRKHS) is characterized by thecongenital absence of the vagina and a variety of Müllerian duct anomalies, http://humrep.oxfordjournals.org/cgi/content/full/19/5/1201

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription* to Human Reproduction Online. * Please note that articles prior to 1996 are not normally available via a current subscription. In order to view content before this time, access to the Oxford Journals digital archive is required. Alternatively, you may purchase short-term access on a Pay per Article basis. Please see below for more details. Full Text Ulrich et al. Hum. Reprod.. This Article Abstract Full Text (PDF ) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Request Permissions PubMed PubMed Citation Articles by Ulrich, U. Articles by Rhiem, K. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password?

58. Laparoscopic Management Of Asymmetric Mayer-Rokitansky-Kuster-Hauser Syndrome -- mayerrokitansky-kuster-hauser (MRKH) syndrome is a partial or completeabsence (agenesis) of the uterus with an absent or hypoplastic vagina. http://humrep.oxfordjournals.org/cgi/content/abstract/10/2/369

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in: ISI Web of Science (12) Request Permissions PubMed PubMed Citation Articles by Chapron, C. Articles by Dubuisson, J. B. ARTICLES Laparoscopic management of asymmetric Mayer-Rokitansky-Kuster-Hauser syndrome C Chapron, P Morice, MD La Tour, X Chavet and JB Dubuisson Service de Chirurgie Gynecologique, Clinique Universitaire Baudelocque, C.H.U. Cochin Port-Royal, Paris, France. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a partial or complete absence (agenesis) of the uterus with an absent or hypoplastic vagina. Until now, the recommended treatment, when resection of a rudimentary horn was indicated, was laparotomy. We report a case of MRKH syndrome in which

59. Forum Médical - Syndrôme De Mayer Rokitansky Kuster Hauser Translate this page Le syndrome de mayer rokitansky kuster hauser est le motif de 1/20 000 consultationsdans les services de gynécologie hospitaliers. http://forums.remede.org/externat_et_ecn/sujet_4609.html

InitBulle("#000000","#FFFFFF","#CCCCCC",1); // InitBulle(couleur de texte, couleur de fond, couleur de contour, taille contour) Sommaire Contacts Documents Sites ... Forums - 81 connectés sur le site - Besoin d'aide ? Forums médicaux Externat et ECN S'enregistrer Identification Rechercher FAQ Vous n'êtes pas identifié Nouveaux messages depuis le : 09/09/05 à 12:28 Stats des forums Tous les forums P2, D1, Externat, ENC Externat et ECN Auteur : Sujet : Syndrôme de Mayer Rokitansky Kuster Hauser Ptithom Shrek Moderator Messages : 2226 Enregistré : 17 Aug 2002 Statut : Déconnecté Vie réelle : Thomas Bony - 24 ans Pays : France Domaine : Médecine Niveau : DCEM3 Fac : LIMOGES posté le 11/05/03 à 21:42 Une infirmière de Limoges a fait un groupe de soutien sur le Syndrôme de Mayer Rokitansky Kuster Hauser, elle voudrait que les étudiants en médecine soient sensibilisés sur ce syndrôme. Elle m'a donné un document dessus, je vous le transmet. Merci de sa part. Autres dénominations : • Agénésie utéro-vaginale • Aplasie mullérienne (canaux de Müller) • Aplasie utéro-vaginale Canaux de Müller : Nom des structures présentes chez l’embryon qui vont donner les trompes de Fallope et une partie du vagin. Il s’agit d’une formation tubulaire paire (des deux côtés) qui va s’atrophier chez l’homme et se transformer chez la femme en vagin, en utérus et en trompe de Fallope.

60. AIS (Androgen Insensitivity Syndrome) Support Group 5alpha-reductase deficiency, Leydig cell Hypoplasia,mayer-rokitansky-kuster-hauser (MRKH) syndrome, Mullerian dysgenesis, Mullerianduct aplasia, http://www.medhelp.org/www/ais/

Welcome to the Adrogen Insensitivity Syndrome Support Group's Web Site. Androgen Insensitivity Syndrome AIS is a condition that affects the development of reproductive and genital organs. Both men and women usually have at least one X chromosome, which contains a gene that gives their bodies the capacity to recognise and react to masculinizing hormones (androgens). Men usually have a Y chromosome as well, which codes for the production of androgens and the inhibition of female internal organ development. Women with AIS have a functioning Y chromosome (and therefore no female internal organs), but an abnormality in the X chromosome that renders the body partially or completely incapable of recognising the androgens produced, therefore allowing the default external genital development along female lines. Other related conditions, based on different chromosomes, also disrupt the normal pathway of androgen action, resulting again in a female phenotype. The Support Group We are a support group providing information and support to young people and adults with complete and partial Androgen Insensitivity Syndrome, and to parents of AIS youngsters. We also support those affected by Swyer's syndrome (XY gonadal dysgenesis), 5-alpha-reductase deficiency, Leydig cell Hypoplasia, Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, Mullerian dysgenesis, Mullerian duct aplasia, vaginal atresia, and other related conditions. Please note that AIS is also known as Testicular Feminisation (or Feminization).

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