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41. Plastic Surgical Nursing : Vaginal Reconstruction In Adolescent Females With May
Plastic Surgical Nursing Vaginal Reconstruction in Adolescent Femaleswith mayerrokitansky-kuster-hauser syndrome. @ HighBeam Research.
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Start P Plastic Surgical Nursing March 22, 2001 ... Vaginal Reconstruction in Adolescent Females with Mayer-Rokitansky-Kuster-Hauser Syndrome.
Vaginal Reconstruction in Adolescent Females with Mayer-Rokitansky-Kuster-Hauser Syndrome.
Plastic Surgical Nursing; March 22, 2001; LeRoy, Suzanne
LeRoy, Suzanne
Plastic Surgical Nursing
March 22, 2001
mrkh syndrome, vaginal reconstruction, mayer-rokitansky-kuster-hauser syndrome, vaginal agenesis, patient, american journal, obstetrics, body image, vagina, patients, congenital absence, gynecology, see table, sexual activity, external genitalia
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by
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43. Vaginal Atresia
VAGINA, ABSENCE OF VAGINAL ATRESIA ROKITANSKI kuster - hauser syndrome; RKH syndrome;VON mayer - rokitansky - kuster ANOMALY; MRK ANOMALY; UTERUS BIPARTITUS
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... 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 ) ...

44. Teen Growth, The Teen Resource For Advice, Health Information, Social Interactio
Q I have mayerrokitansky-kuster-hauser syndrome/Muellerian aplasia.What is the difference is between MRKH and Muellerian aplasia.
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45. UCL Hospitals - Links To Other Useful Web-sites
This is also called rokitansky syndrome, MRKH (mayerrokitansky-kuster-hauser)syndrome, mullerian dysgenesis and mullerian dysplasia.
http://www.uclh.org/links/index.shtml

uclh

useful links

These links to other external web-sites have been compiled for your information. Please note, UCL Hospitals has no responsibility for the content of these sites. Broken link? Let us know Last updated: June 26 2001 Archives
Other local trusts and NHS Organisations

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Miscellaneous
Archives
Manuscripts and rare books department at UCL Library For the archives of University College Hospital. London Metropolitan Archives For the records of The Elizabeth Garrett Anderson Hospital. The archives of The Middlesex Hospital, St Peter's and St Paul's hospitals, The Hospital for Women, Soho, and The National Temperance Hospital are stored at UCL Hospitals. More information can be found on our archives pages
Other local trusts / NHS organisations:
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46. AIS (Androgen Insensitivity Syndrome) Support Group
syndrome (XY gonadal dysgenesis), 5alpha-reductase deficiency, Leydig cell Hypoplasia,mayer-rokitansky-kuster-hauser (MRKH) syndrome, Mullerian dysgenesis
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).

47. Introduction
syndrome (XY Gonadal Dysgenesis), 5alpha Reductase Deficiency, Leydig Cell Hypoplasia,mayer-rokitansky-kuster-hauser (MRKH) syndrome, Mullerian Dysgenesis
http://www.medhelp.org/www/ais/01_INTRO.HTM
Androgen Insensitivity Syndrome Support Group Website
(If you came to this page directly, please go to our entry page by clicking here.)
Androgen Insensitivity Syndrome
Support Group (AISSG)
[this page last updated 28 July 2002] UK Group
Registered UK Charity No. 1073297
Affiliated to Contact a Family Rare Disorders Alliance-UK
Genetic Interest Group (GIG), Long Term Medical Conditions Alliance
and
International Alliance of Patients' Organizations (IAPO)
US Group
Registered IRS [501(c)3 Organization] No. 37-1407648
Canadian Group
Charitable Business No. 88977 6142 RR0001 Spanish Group Fiscal Identification (C.I.F.) G63220958 Before meeting others affected.... (Picasso - 'On the Beach') .... After meeting, and much talking (Picasso - 'Three Bathers') The Androgen Insensitivity Syndrome Support Group (AISSG) is a consortium of worldwide support groups that owe their origins to the UK-based group which was started in 1988 (formalised in 1993). We provide information and support to young people and adults with complete and partial Androgen Insensitivity Syndrome (AIS) - old name Testicular Feminization Syndrome or Testicular Feminisation Syndrome (TFS) - 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.
Aims of the Group

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50. Dictionary Definition Of ROKITANSKY, KARL FREIHERR VON
person Austrian pathologist, 18041878. See rokitansky s disease, rokitansky shernia, rokitansky-Aschoff sinuses, mayer-rokitansky-kuster-hauser syndrome.
http://www.dictionarybarn.com/ROKITANSKY-KARL-FREIHERR-VON.php
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51. Dictionary Definition Of KUSTER
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Herman, early 20th century German gynecologist.
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52. International MRKH Syndrome Meetup Day
International MRKH syndrome Meetup Day. in 16 Days. WHAT. Meetup with otherlocal women dealing with mayerrokitansky-kuster-hauser syndrome. WHEN.
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WHAT Meetup with other local women dealing with Mayer-Rokitansky-Kuster-Hauser Syndrome. WHEN Wednesday, June 9 @ 6:00PM
(2nd Wednesday of every month.) WHO Women with MRKH Syndrome Worldwide (and friends.) So far, have signed up. AGENDA T.B.D. More info.
Join other Women with MRKH Syndrome near you!
MRKH Syndrome Meetups can happen in up to 646 cities worldwide on the same day. Enter your location to find the one near you: writeForm("horiz") US Residents, enter your 5-digit Zip Code: Non-US Residents, select your city: Select Your City Antarctica: South Pole, Antarctica Argentina: Buenos Aires, Argentina

53. International MRKH Syndrome Meetup Day
International MRKH syndrome Meetup Day. in 25 Days. WHAT. Meetup with otherlocal women dealing with mayerrokitansky-kuster-hauser syndrome. WHEN.
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54. AJR -- Abstracts: Strubbe Et Al. 160 (2): 331
ARTICLES. mayerrokitansky-kuster-hauser syndrome distinction between two formsbased on excretory urographic, sonographic, and laparoscopic findings.
http://www.ajronline.org/cgi/content/abstract/160/2/331
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Rolland, R. Download to Citation Manager
ARTICLES
Mayer-Rokitansky-Kuster-Hauser syndrome: distinction between two forms based on excretory urographic, sonographic, and laparoscopic findings
EH Strubbe, WN Willemsen, JA Lemmens, CJ Thijn and R Rolland
Department of Radiology, Rijnstate Hospital, Arnhem, The Netherlands. OBJECTIVE. The purpose of this study was to discriminate typical (type A) from atypical (type B) Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome (congenital absence of vagina and uterus) and determine their association with renal anomalies and ovarian disease. MATERIALS AND METHODS. The excretory urographic, sonographic, and laparoscopic findings in 91 patients with MRKH syndrome were compared retrospectively. Symmetric muscular buds and fallopian tubes were diagnostic of type A, and asymmetric muscular buds

55. Malattie Rare E Genetiche Lettera "U"
Translate this page Retinitis Pigmentosa and Congenital Deafness/Usher syndrome (US)•••{M ducanal de muller galactosemie•mayer rokitansky kuster hauser, Síndrome de
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57. KUSTER Definition
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Sindrome mayerrokitansky-kuster-hauser. 1995, 37, 114-17. 3. Giatras KI et al.Laparoscopy for pelvic pain in the mayer-rokitansky-Küster-hauser syndrome.
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Adam J. Sybilski, Danuta Kurowska
z Oddzia³u Dzieciêcego Centralnego Szpitala Klinicznego MSWiA w Warszawie
Ordynator Oddzia³u: lek. med. Aleksandra £agun

Wady narz±dów p³ciowych u dziewcz±t s± tematem rzadko poruszanym w dyskusjach pediatrycznych. Dotycz± one zaburzeñ w obrêbie przewodów p³ciowych, ³±cznie z pochw±. Ocenia siê, ¿e wady rozwojowe pochwy i macicy wystêpuj± u 0,5-0,8% badanych pacjentek z zaburzeniami ginekologicznymi, choæ zastosowanie badañ dodatkowych w postaci ultrasonografii czy laparoskopii zwiêksza ten odsetek do 2,9% a nawet 8,6% (7). Jedn± z czê¶ciej wystêpuj±cych wad rozwojowych narz±du rodnego jest wrodzony brak pochwy i macicy zwany zespo³em Mayer-Rokitansky-Küster (zespó³ M-R-K), w pi¶miennictwie pojawiaj±cy siê te¿ jako zespó³ Müller-Phillipa (6, 8, 10).
Zespó³ Mayer-Rokitansky-Küster zosta³ po raz pierwszy opisany przez C.A.J. Mayera w 1829 roku i nazwany przez niego "uterus bipartitus". Nastêpnie C. von Rokitansky w 1838 roku zapo¿yczy³ ten termin do okre¶lenia wrodzonego braku macicy i pochwy bez wzglêdu na postaæ tej wady. W 1910 roku H. Küster przedstawi³ przegl±d pi¶miennictwa na temat tej wady, podaj±c jednocze¶nie wiele jej wariantów (10).

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This page was last updated on 4/20/04. If you know of errors please click here to let us know. Britain's UK Intersex Association: writings by intersex individuals and excellent links: http://www.ukia.co.uk/ Intersex Initiative: articles, first person stories and a great Intersex FAQ page. Also, their speakers bureau http://www.ipdx.org/ Intersex Society of North America: information, bibliographies and articles regarding gender and gender reassignment http://www.isna.org/ A Path to Greater Understanding: This web page introduces you to ten people whose stories may surprise you. If you have always wondered what "transgender" and "intersex" meant, check this page out. If you have wondered whether there was a place in religious institutions for gender-different people, check this page out and consider ordering the booklet by the same name: http://www.madeinimage.org What is Intersexuality? This resource was put together by PFLAG national for its local chapters, answering that question:

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