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AISNederland - Links Naar Andere Websites Androgeen Ongevoeligheid Syndroom. mrkh (MayerRokitansky-Küster-Hauser. mrkh (Mayer-Rokitansky-Küster-Hauser)komt bij ongeveer 1 op de 10.000 vrouwen voor. http://www.aisnederland.nl/links.html
Extractions: andere websites Vrouwen met AOS* hebben een intersekse-aandoening. Dat wil niet zeggen dat we ons 'een beetje man en een beetje vrouw' voelen. Het is slechts de van oudsher gebruikelijke medische term waarmee wordt aangegeven dat iemand zowel vrouwelijke als mannelijke lichaamskenmerken heeft. Binnen AISNederland zijn diverse intersekse-aandoeningen vertegenwoordigd die als gemeenschappelijk kenmerk hebben dat je XY-chromosomen hebt maar als vrouw wordt geboren. Er zijn echter tientallen andere intersekse-aandoeningen. Androgeen Ongevoeligheid Syndroom Klinefelter Syndroom Adrenogenitaal Syndroom Interseksualiteit algemeen ... Algemeen medische links Bij AOS (Androgeen Ongevoeligheid Syndroom) is een vrucht met XY-chromosomen geheel of gedeeltelijk ongevoelig voor androgenen, waardoor het lichaam zich niet in een mannelijke richting kan ontwikkelen. De meeste mensen met AOS hebben overeenkomstig hun lichamelijke kenmerken een vrouwelijke genderidentiteit. Als een lichaam geheel ongevoelig is voor androgenen en daardoor in het geheel geen mannelijke uiterlijke kenmerken heeft, is sprake van Complete AOS (CAOS). Bij een gedeeltelijke ongevoeligheid kan het lichaam gedeeltelijk vermannelijken en wordt gesproken over Partieel AOS (PAOS). De Engelstalige naam voor AOS is Androgen Insenitivity Syndrome (AIS). http://www.AISNederland.nl/
Forum2: Beitrag Lesen mrkh Schweiz die homepage ist wieder da unter www.mrkh.ch mit http://www.frauenarzt-infos.de/Foren/Forum2/read.php3?id=63
Forum2: Beitrag Lesen mrkh Schweiz www.mrkh-syndrom.de/ habe die seite gelöscht weil es http://www.frauenarzt-infos.de/Foren/Forum2/read.php3?id=62
Rnglinksinterseksualiteit mrkh (MayerRokitansky-Küster-Hauser) mrkh komt bij ongeveer 1 op de 10.000 vrouwenvoor. www.surrogacy.com Amerikaanse supportgroep voor vrouwen met mrkh. http://www.rng.nl/html/rnglinksinterseksualiteit.htm
Extractions: Bij interseksualiteit heeft een kind kenmerken van zowel het vrouwelijk als het mannelijk geslacht. Vaak wijkt het chromosomenpatroon af van hetgeen het lichaam doet vermoeden, bijvoorbeeld XY-chromosomen en een vrouwelijk lichaam. In veel gevallen, maar niet alle, wordt interseksualiteit veroorzaakt door een gen-defect. Interseksualiteit is niet hetzelfde als transseksualiteit. Meestal is de lnterseksualiteit al bij de geboorte duidelijk en wordt op basis van de mate van vermannelijking of vervrouwelijking een geslacht toegewezen. In een beperkt aantal gevallen maakt een interseksueel kind op latere leeftijd een eigen keuze die niet overeenkomt met de oorspronkelijke geslachtstoewijzing. Medisch en sociaal wordt dit gezien als een terugkeer naar het oorspronkelijk al aanwezige, maar verkeerd geïnterpreteerde geslacht.
Www.surrogatealternative.com/mrkh.htm DrRecommend amenorrheaHome Health Women s_Health Menstruation Amenorrhea mrkh1.Cytologic Findings in a Neovagina Short medical article about http://www.surrogatealternative.com/mrkh.htm
Extractions: Jan 31, 2004 As reported in The Times of India and elsewhere, a British woman gave birth to twin boy and girl who are genetically her grandchildren. The grandmother agreed to become the surrogate mother because the twins' genetic mother had a congenital condition in which her uterus and a few other reproductive organs are missingbut her ovary was intact and could provide an ova for IVF treatment. Her condition is known as MRKHMayer-Rokitansky-Kuster Hauser syndrome (simply referred to as the "Rokitansky syndrome" in the article)and occurs in about one in 5,000 women. For more information about MRKH, see MRKH.org
MRKH From Linkspider UK Health Directory mrkh by Linkspider UK, mrkh links and mrkh topics from our Healthdirectory. Helping Directory Topic mrkh assoicated to Health. http://linkspider.co.uk/Health/Women'sHealth/Menstruation/Amenorrhea/MRKH/
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Absence Of The Uterus (Vaginal Agenesis) Girls with vaginal agenesis (also referred to as mullerian agenesis, Rokitanskysyndrome, and MayerRokitansky-Kuster-Hauseror mrkhsyndrome) usually http://www.drspock.com/article/0,1510,6204,00.html
Extractions: Many girls and women have never heard of vaginal agenesis, a condition in which a girl is born without a uterus. And yet it's fairly common, affecting 1 out of every 4,000 girls. The condition can be traced to the fetal stage of development, when the uterus and upper vagina do not form properly. Abnormalities of the kidneys or bones may occur as well. The external, visible genital area of girls with this condition looks totally normal; it's only upon closer examination that a healthcare practitioner will discover a very shallow vagina and, after further testing, the absence of a cervix and uterus. Occasionally there is a small, nonfunctional "remnant uterus." Ultrasound or magnetic resonance imaging (MRI) scan is usually needed to be certain about this diagnosis. Before sexual intercourse is possible, most girls with vaginal agenesis must undergo a procedure to lengthen the vagina. This generally is best accomplished with the dilation method, where a young woman is taught how to put pressure on the inside of her vagina with a dilator, as instructed by a doctor or nurse. Most girls feel ready to take on this responsibility between the ages of 15 and 20. Gradually, after a few months of daily exercises, the vagina becomes deeper and wider, to make intercourse possible.
Mermaids: Links And Search Engines XY gonadal dysgenesis (Swyer s syndrome) and 5 alpha reductase deficiency, and alsoXX females with Mayer Rokitansky Kuster Hauser (mrkh syndrome, Mullerian http://www.mermaids.freeuk.com/links.html
Extractions: Kenneth's website Alek's Site Claire's Site Vicky's Site Mermaids Mailing List - Open to young transgendered people between ages 12 and 19. Mermaids-UK-Parents - MermaidsUK Parents is a UK-based support, information and friendship list for the parents or carers of 'gender variant' children and teenagers, up to and including the age of 18 years. These young people will all have some kind of gender identity issue - of which some may be transient, some permanent - either way, the situation can be a difficult one for all concerned TSTalk-UK - For Transsexual people only (and others invited by the moderators) Transsexual-UK FTM Network (UK) Gender Trust - An organisation for Transsexual People and Transgenderists. Grampian Gender Group Antijen - The Antijen list is a place for young transsexual kids to talk and try to sort the whole mess out. We talk about parents, work, school, doctors, new experiences, ways to cope and grow. It's a place to find out information, meet a few people, and generally feel like you're a little less alone in all of this. It's scary sometimes, and it's always good to have a place to talk things through. Manchester Parents Group is a support and information network for parents, families, and friends of lesbians, bisexuals and gay men.
Mayer-Rokitansky-Küster-Hauser Syndrome Disorders that cause congenital scoliosis include MayerRokitansky-Küster-Hauser(mrkh) syndrome. http://www.medscape.com/viewarticle/410500
Program Esther Morris, author of The Missing Vagina Monologue, on her experience withmrkh Syndrome, a notso-rare physical condition that causes women to be born http://www.gendertalk.com/real/300/gt342.shtml
Extractions: var mp3_server="'http://gendertalk.tgforum.com/gt" var mp3_server_no_gt="'http://gendertalk.tgforum.com/" var mp3_downserver="'ftp://gendertalk.tgforum.com/gt" var ra_server="'http://gendertalk.tgforum.com/gt" var old_ra_server="'ftp://gendertalk.tgforum.com/gt" var rita_server="'http://gendertalk.tgforum.com/" var alt_mp3_server="'http://www.gendertalk.com/mp3/gt" var prog_num=342 var month="December" var date=31 var year=2001 document.write("GenderTalk #") document.write(prog_num) document.write(", ") document.write(month) document.write(" ") document.write(date) document.write(", ") document.write(year) document.write("")
Program RealAudio (5 MB). Esther Morris, on the response to her Missing VaginaMonologue activism from Eve Ensler and the mrkh intersexual community. http://www.gendertalk.com/real/350/gt359.shtml
Extractions: var mp3_server="'http://gendertalk.tgforum.com/gt" var mp3_server_no_gt="'http://gendertalk.tgforum.com/" var mp3_downserver="'ftp://gendertalk.tgforum.com/gt" var ra_server="'http://gendertalk.tgforum.com/gt" var old_ra_server="'ftp://gendertalk.tgforum.com/gt" var rita_server="'http://gendertalk.tgforum.com/" var alt_mp3_server="'http://www.gendertalk.com/mp3/gt" var prog_num=359 var month="May" var date=13 var year=2002 document.write("GenderTalk #") document.write(prog_num) document.write(", ") document.write(month) document.write(" ") document.write(date) document.write(", ") document.write(year) document.write("")
JN 2001; Vol.14 N°4: 316-318 ABSTRACT MayerRokitanski-Küster-Hauser (mrkh) syndrome, is a rare disordercharacterized by the congenital absence of the uterus and vagina. http://www.sin-italia.org/jnonline/Vol14n4/316.html
Extractions: Table of Contents Case report JNEPHROL 2001; 14: 316-318 Renal abnormalities in Mayer-Rokitanski-Küster-Hauser syndrome Carlo Basile , Vittorio De Michele Nephrology and Radiology Units, Hospital of Martina Franca - Italy ABSTRACT: Mayer-Rokitanski-Küster-Hauser (MRKH) syndrome, is a rare disorder characterized by the congenital absence of the uterus and vagina. The prevalence has been reported as one in 4000 5000 female births. Patients with MRKH syndrome have a 46.XX karyotype and normal secondary sex characteristics. The external genitalia appear normal, but only a shallow vaginal pouch is present. Ovarian function is normal. A 54-year-old woman came to our observation for the treatment of arterial hypertension. Her history involved primary amenorrhea and sterility. She had undergone abdominal and pelvic sonography as a routine screening and they had shown the absence of the uterus, left renal agenesis and a contralateral pelvic kidney. These findings were confirmed by urography and CT scan of the abdomen. Gynecologic examination showed a small vaginal pouch (2 cm). Thus, the diagnosis of MRKH syndrome with associated congenital anomalies of the upper urinary tract was made for the first time in this lady at the age of 54 years. Associated congenital anomalies of the upper urinary tract are reported to occur in 30 40 % of all cases of MRKH syndrome. No specific figures are available on what percentage of women with missing kidney might also have MRKH syndrome. However, in 40 50 % of patients with renal agenesis, an associated genital anomaly has been found.
MRKH : Meddie Health Search A case of MayerRokitansky-Kuster-Hauser syndrome CT findings Mayer-Rokitansky-Kuster-Hauser syndrome (mrkh) is a rare syndrome characterisedby complete or partial absence of the vagina, uterus and proximal fallopian http://www.meddie.com/Women_s_Health/Menstruation/Amenorrhea/MRKH/
Mayer-Rokitansky-Kuster-Hauser Syndrome View mrkh Syndrome Images. MRI of the abdomen and pelvis T1 axial and T2 axialof the pelvis were obtained, confirming the diagnosis of mrkh syndrome. http://cats.med.uvm.edu/cats_teachingmod/radiology/radiology_html/teaching/radio
Extractions: The patient is a 16 year old white female who had undergone normal development of secondary sex characteristics, yet remained amenorrheic. Her pelvic exam was notable for pain, and the cervix was not visualized on speculum exam. Hormonal tests (estradiol, FSH, LH, TSH, prolactin) were all within normal limits for an adolescent female in the follicular stage. This enabled the physician to rule out androgen insensitivity (testicular feminization), and suggest that a pituitary tumor was not the cause of amenorrhea. An ultrasound exam was attempted (study not available). Transabdominally, the uterus was not identified. An endovaginal US exam could not be performed, secondary to pain. She was referred to MR for evaluation of the pelvic organs. Radiographic Findings:
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
Book Thoughts - Sitemap voltage reading mrives christmas book notes mrj os debugging mrjames k elrod mrjonesthe master of all prayers mrjusticehooper mrkeith pain movie mrkh mrkh and http://www.book-thoughts.com/s/s_bvj.html
WOMENS-HEALTH Messages For July, 2000: MRKH mrkh. From Melissa (anonymous@obgyn.net) Sun, 9 Jul 2000 231739 0500 (CDT) Ihave mrkh. I am looking for a specialist in the Greenville South Carolina area. http://forums.obgyn.net/forums/womens-health/WHF.0007/0532.html
Extractions: Sun, 9 Jul 2000 23:17:39 -0500 (CDT) I have MRKH. I am looking for a specialist in the Greenville South Carolina area. Just wondering if there is anyone that might have the name of one nearby. Enter search keywords: Returns per screen: Require all keywords: Return to Report TECHNICAL Problems ONLY to: webmaster@obgyn.net
