Www.myspace.com/mrkh MySpace Music Profile Mark Hansen - Christian - WEST JORDAN, UTAH, US. http://www.myspace.com/mrkh
Extractions: Mark Hansen General Info Member Since April 18, 2005 Band Website markhansenmusic.com Band Members Mark Hansen - Singer, Songwriter, Guitarist, Producer, with occasional help in the studio from friends, like: John Newman - Co-producer, Arranger, Trumpeter Morey Day - Percussion, Drum programming Steve Hill - Drums Influences Boston, Rush, Yes, Nazareth, Kansas, Genesis, Ozzy, Motley Crue, Bach, Greg Simpson, Metallica, Offspring Sounds Like Each song is a different exploration in style, all rooted in Classic Rock. Record Label Self-Produced
JN 2001; Vol.14 N°4: 316-318 Patients with mrkh syndrome have a 46.XX karyotype and normal secondary sex The coexistence of renal agenesis and the mrkh syndrome has in fact been http://www.sin-italy.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.
Extractions: Pediatrics for Parents , Jan, 2002 by Niki Taylor Girls who have not started their periods by the appropriate age should be checked for Mayer Rokitanksy Kuster Hauser Syndrome (MRKH). MRKH, named after four men who studied this birth defect, describing a female born without a uterus or only part of one, no cervix, and no vagina or a very short one and normal ovaries. Doctors can't usually tell anything by a pelvic exam since the vagina is closed off. Ultrasound, magnetic resonance imaging (MRI), and laparoscopy are all ways to determine what reproductive organs the females have. These are usually done after blood tests show the woman is genetically a female.
Extractions: Pediatrics for Parents , Jan, 2002 by Niki Taylor Girls who have not started their periods by the appropriate age should be checked for Mayer Rokitanksy Kuster Hauser Syndrome (MRKH). MRKH, named after four men who studied this birth defect, describing a female born without a uterus or only part of one, no cervix, and no vagina or a very short one and normal ovaries. Doctors can't usually tell anything by a pelvic exam since the vagina is closed off. Ultrasound, magnetic resonance imaging (MRI), and laparoscopy are all ways to determine what reproductive organs the females have. These are usually done after blood tests show the woman is genetically a female.
The MAGIC Foundation Mayer Rokitansky-Kuster-Hauser (mrkh) syndrome is an uncommon variation in the Females with mrkh syndrome have functioning ovaries, normal external http://www.magicfoundation.org/www/docs/107.290
Extractions: What is Mayer-Rokitansky-Kuster-Hauser Syndrome? Mayer- Rokitansky-Kuster-Hauser (MRKH) syndrome is an uncommon variation in the prenatal development of the female genital tract. Its features include an absent or very short vagina and a uterus that can be absent or immaturely formed. Females with MRKH syndrome have functioning ovaries, normal external genitalia and the typical, 46, XX, female chromosome pattern. Breast development and growth of pubic hair are also normal. Associated renal and/or skeletal abnormalities are common. MRKH syndrome is also known as Mullerian (female internal sex organs) Agenesis (no growth) syndrome (a group of related medical findings). How often does MRKH syndrome occur? The incidence of MRKH syndrome is approximately 1 in 4,000 - 5,000 female births. Although it has been determined that the absence of a vagina and uterus is a result of the Mullerian ducts failing to form properly early in embryonic development, its underlying cause is unknown. When is a diagnosis of MRKH syndrome made? The normal external appearance of MRKH females makes it difficult to diagnose until puberty - often when a girl visits a physician because she has not started to menstruate. In some cases, a young woman may have attempted unsuccessfully to have intercourse. The average age of diagnosis is between 15 and 18 years, although occasionally a girl may be diagnosed at birth or during childhood because of other health problems. A pelvic ultrasound may be used to see the presence or absence of the uterus and its condition. Doctors might use laparoscopy, a surgical technique that allows the doctor to view the inside of the abdominal cavity, to determine the presence, absence and/or condition of the internal female sex organs. Blood work is usually done to determine a chromosome pattern and to test for hormonal levels.
Intersexual Organizations mrkhgrrls · mrkh List. If you have mrkh Mayer-Rokitansky-Kuster-HauserSyndrome or you are the mother of someone who does, you are welcome to join http://www.rachelmiller.info/linkso3f-inter.htm
Extractions: Intersexual Androgen Insensitivity Syndrome Support Group (AISSG) On Boxing Day 1994, an AIS woman in her mid-30s was searching for information on AIS in her local medical library on the west coast of America, having received the usual (at that time) 'blank wall' from doctors when it came to requesting information and contact with others. She was pleased to find an article, Once a Dark Secret , in the British Medical Journal and to find that the subsequent issue of the journal contained a response letter from a doctor. She photocopied the pages, and was reading them in her car at traffic lights when she realised that she'd failed to copy an additional page which contained the major part of second response letter from, as she put it, "....much more importantly, another AIS woman!" She rushed back to the library and found the missing page, which to her delight also contained the phone number for the AIS Support Group in the UK. She made contact just as the group was making the first issue of its newsletter, ALIAS, available - and in time to attend the UK group's first meeting in March 1995. And on her return to the US she started to set up a group there. Bodies Like Ours - Peer Support and Information for people born with a body that is different.
MRKH UK - Support For Sufferers And Family The MayerRokitansky-Kuster-Hauser (mrkh) syndrome without and A multidisciplinary study was conducted on a total of 100 women with congenitalabsence of vagina an http://www.webmentorlibrary.com/gateway.asp?site=http://www.mrkh.org.uk
Entrez PubMed PATIENT(S) Six consecutive cases of mrkh over a period of 12 months. MAIN OUTCOME MEASURE(S) Clinical and laboratory features of mrkh and presence of http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
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
Aanmelding Mailinglist MRK (MRKH) Syndroom Aanmelding Mailinglist MayerRokitansky-Küster-Hauser Syndroom. Na invullen enversturen, wordt u toegevoegd aan de lijst. http://www.freya.nl/frmmrk.htm
Extractions: Als het aanmelden via dit formulier onverhoopt niet mocht lukken, stuur dan een mail met uw gegevens naar lijstbeheer@freya.nl -deze gegevens zijn gelijk uw introductie op de lijst- MRK Voornaam en geboortejaar Sinds wanneer bekend Sinds wanneer in medisch circuit Eventuele medische ingrepen Waar onder behandeling en bij wie e-mail adres voor de mailinglist Lidnummer Freya (niet verplicht)
Aanmelding Mailinglist MRK (MRKH) Syndroom Aanmelding Mailinglist Asherman Syndroom. Na invullen en versturen, wordt utoegevoegd aan de lijst. Dit gebeurt door de lijstbeheerder of webmaster. http://www.freya.nl/frmash.htm
Extractions: Als het aanmelden via dit formulier onverhoopt niet mocht lukken, stuur dan een mail met uw gegevens naar lijstbeheer@freya.nl -deze gegevens zijn gelijk uw introductie op de lijst- Asherman Voornaam en geboortejaar Sinds wanneer bekend Sinds wanneer in medisch circuit Eventuele medische ingrepen Waar onder behandeling en bij wie e-mail adres voor de mailinglist (exact) Lidnummer Freya (niet verplicht)
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All Showcase - MRKH WOMENSHEALTH Messages for July, 2000 mrkhNext in thread William F. von Almen, II, MD, FACOG Re mrkh I have mrkh.I am looking for a specialist in the Greenville South Carolina area. http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/M/MRKH/
Extractions: Sat, 21 Mar 1998 21:34:14 -0600 (CST) I have MRKH (congenital absence of the vagina and infantile uterus). My mother had seven pregnancies, all girls, of which I was the oldest. Two of my sisters were born with spina bifida and died at a young age. One sister has no sense of smell (from birth). Another sister went through premature ovarian failure at age 26, her karyotype includes a missing leg on one of her x chromosones. My question is: could there be a reason all these congenital abnormalities occured in one family? I have read of connections between MRKH and spinal abnormalities. I am aware of one woman with MRKH who has no sense of smell. Dr. Daniel Cramer of Harvard has published articles on his theory that a galactose processing deficiency can cause both MRKH and premature ovarian failure. Do you have any suggestions for me on who might be appropriate to contact with this kind of question? Thank you, Pat
ScienceDaily -- Browse Topics: Health/Women's_Health/Menstruation/Amenorrhea/MRK Bioline International Official Site (site updated regularly)mrkh syndrome is a rare but widely discussed developmental failure of in part orwhole of the The mrkh syndrome occurs in 1 of 4000-5000 female births. http://www.sciencedaily.com/directory/Health/Women's_Health/Menstruation/Amenorr
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Syndrome Mrkh: Chantal Translate this page http://www.casediscute.com/2004/001_femme/messages/98.html
