Extractions: 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 ) ...
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
Extractions: Miscellaneous 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 NHS Direct National Health Service (NHS.UK) Department of Health London Regional Office, NHS Executive ... Back to top Camden Islington Back to top Open Government Back to top National Association of Councils for Voluntary Service National Centre for Volunteering Back to top Royal Free and University College Medical School ... Back to top Royal College of Radiologists Royal College of Psychiatrists Royal College of Obstretrics and Gynaecology Royal College of Pathologists ... Royal College of General Practitioners The hospital school
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/
Extractions: 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).
Extractions: (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
Extractions: Middle East, Middle East mrkh news mrkh the Middle East, fundamentalism fundamentalist, Islam, Islamic, Muslim, human rights, Islamic law, Arab World, mrkh World, news from Egypt, news about Egypt, Egypt news, Egyptian news, news mrkh Nasser, Sadat, Mubarak, mrkh Israel, mrkh desert, camel, pyramid, oriental, women's mrkh development, third world, Egypt, Africa, mrkh Womens' rights, Sudan, Somalia, Libya, business, Syria, mrkh Lebanon, Algeria, Saudi Arabia, Yemen, the Arabian Gulf, mrkh Gulf, the Persian Gulf, Turkey, mrkh mrkh
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
Dictionary Definition Of KUSTER Translate this page See mayer-rokitansky-kuster-hauser syndrome, rokitansky-kuster-hauser syndrome.Please select first two letters of word you are looking for. http://www.dictionarybarn.com/KUSTER.php
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. http://mrkh.meetup.com/
Extractions: @import url("http://www.meetup.com/style/common.css"); @import url("http://www.meetup.com/style/topic.css"); @import url("http://www.meetup.com/style/hide-from-ie-mac.css"); @import url("http://www.meetup.com/style/images.css"); Your Meetup now has its own Message Boards! Join the conversation! Meetup Home Discuss Meetup.com Sign In ... MRKH Syndrome WHAT Meetup with other local women dealing with Mayer-Rokitansky-Kuster-Hauser Syndrome. WHEN Wednesday, June 9 @ 6:00PM Meetup Members ... Links 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
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. http://mrkh.meetup.com/?change=1&localeId=283
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
Extractions: 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
Malattie Rare E Genetiche Lettera "U" Translate this page Retinitis Pigmentosa and Congenital Deafness/Usher syndrome (US){M ducanal de muller galactosemiemayer rokitansky kuster hauser, Síndrome de http://fmfpc.altervista.org/U.htm
Blackwell Synergy - Cookie Absent CASE REPORT. Laparoscopic extirpation of bilateral rudimentary horns ina patient with a variant of mayerrokitansky-kuster-hauser syndrome. http://www.blackwell-synergy.com/links/doi/10.1046/j.1365-2508.2002.00518.x/full
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KUSTER Definition Herman, early 20th century German gynecologist. See mayerrokitansky-kuster-hausersyndrome, rokitansky-kuster-hauser syndrome. Toys and Blankets. Miami Rooms. http://www.books.md/K/dic/Kuster.php
Archives Savoir Plus Santé sexuelles (GAMS). syndrome DE mayer rokitansky kuster hauser. http://savoirplussante.france2.fr/archives/63680-fr.php
Extractions: 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).
Extractions: 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:
