81. OSTEOPOROSE Translate this page treatment of pelvic pain. Keywords Laparoscopic surgery, mayer-rokitansky-kuster-Hausersyndrome. Introdução. A síndrome de mayer http://www.usp.br/medicina/departamento/g-o/gineco/artigrev4_4.htm

82. Intersex Congenital Adrenal Hyperplasia (CAH) CAH Our Voices Our Stories. MayerRokitansky kuster hauser syndrome. Hypospadias Association of America. http://ochs.bi.org/website/resources/Intersex.html

Robyn's Home Page INTERSEX Intersex Society of North America Bodies Like Ours Transfeminism.org The U.K. Intersex Association ... Androgen Insensitivity Syndrome Support Group (AISSG) AIS Support Group Australia, Inc. Klinefelter Syndrome Support Group Turner's Syndrome Society of the United States XY Turners Genetic Mosaic Support Group Congenital Adrenal Hyperplasia (CAH): CAH Our Voices Our Stories Mayer Rokitansky Kuster Hauser Syndrome Hypospadias Association of America

83. M MarieSainton Disease; @ Marinesco-Sjogren syndrome; @ mayer RokitanskyKuster hauser syndrome; @ McArdle's Disease; @ Measles,Red; @ Measles http://www.ad.com/Health/Conditions_and_Diseases/M/

search Top Categories: MAC @ MPS III @ MRKH @ Machado-Joseph Disease ... @ Myotonic Dystrophy AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

84. AIS Fact Sheet Smith Lemli-Opitz syndrome. XX conditions with some AIS-like features MayerRokitansky kuster hauser (MRKH) syndrome,. Mullerian dysgenesis. Incidence. http://home.vicnet.net.au/~aissg/ais_fact_sheet.htm

AIS Fact Sheet Home Up What's new with the AISSGA? Aims and Policies ... Contact Us This Fact Sheet is an AIS Support Group Australia adaptation of the AISSG(UK) Fact Sheet. The AIS Support Group Australia is a peer support group providing information and support to people with AIS and related intersex conditions and their families. Introduction Up to 8 weeks gestation every foetus, whether of typical male or female chromosomal sex, has the capacity to develop either a male or female reproductive system, and in a typical male (XY) foetus the active intervention of male hormones (androgens) is needed to produce a fully male system. A female body type with female external genitalia is the basic underlying human form. What is AIS? Androgen Insensitivity Syndrome (old name Testicular Feminisation Syndrome) causes an interruption of the foetal development of the reproductive system. In AIS the child is conceived with typical male (XY) sex chromosomes. Embryonic testes develop and start to produce androgens but the body is unable to respond to these androgens to a varying degree. This means that the genitals can vary from completely female if there is no response through to almost completely male if there is a slight insensitivity to androgens or anywhere in between.

85. Gynecology Links Genetic Male (10%). Axis 4 Uterus Mullerian Agenesis (20%) mayerrokitansky-kuster-HauserSyndrome. Primary Amenorrhea Algorithm http://www.fpnotebook.com/GYN69.htm

Home About Links Index ... Editor's Choice Paid Advertisement (click above). Please see the privacy statement Gynecology General Assorted Pages Gynecology Links Gynecology Resources Worksheets Gynecology Notebook Gynecology Links Other Links http://www.4woman.org http://www.pitt.edu/HOME/GHNet/GHWomen.html http://www.womens-health.com/ http://www.ama-assn.org/special/womh/womh.htm Dr. Pranikoffs Ob/Gyn Web Library http://blues.fd1.uc.edu/~pranikjd Search other websites for this topic Search National Library of Medicine PubMed for related articles Search Google for related images or topics Paid Advertisement (click above). Please see the privacy statement Although access to this page is not restricted, the information found here is intended for use by medical providers. Patients should address specific medical concerns with their physicians. Please see the Terms and Conditions . This page was written by Scott Moses, MD, and was last revised 2/12/2003. Please send comments and questions to the editor. Contact information may be found on the page About the Family Practice Notebook This is one page of 3 in this chapter, 172 in this book, and 4212 in the Family Practice Notebook.

86. What Is AIS? - FactSheet AISSGA XX Conditions with some AISlike features. mayer rokitansky KusterHauser (MRKH) syndrome, Mullerian dysgenesis. How Common is AIS? http://www.ftmaustralia.org/pubs/facts/intersex/002.htm

87. WELS Questions And Answers-- Christian Living/Human Behavior - Sexual Behavior Female (XX) conditions with some similarities to AIS mayer rokitansky KusterHauser (MRKH) syndrome, Mullerian dysgenesis, vaginal atresia. http://www.wels.net/sab/qa/behav-sex-05.html

Christian Living/Human Behavior - Sexual Behavior Out of curiosity, how do we (the WELS church) decide who is male and who is female? Can someone with only one sex chromosome be a pastor? Should someone who is androgen insensitive marry a woman or a man? I realize that none of this matters when it comes to salvation, but I thought this issue might be relevant to all the recent sex role questions. A biological intersex condition (BIC) poses a challenge for those striving to follow the Scriptural teachings on proper role relationships. BICs generally consist of a genetic make-up that is contrary to the physical appearance with regard to sexual organs. BICs is a term that generally applies to the following: Androgen Insensitivity Syndrome (AIS), Androgen Resistance Syndrome, Testicular Feminization Syndrome, Feminizing Testes Syndrome, Male Pseudo-hermaphroditism, Morris's Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome (PAIS), Rosewater Syndrome (PAIS), Lubs Syndrome (PAIS). Other male (XY) conditions with some similarities to AIS: 5 alpha-reductase deficiency, 17 keto-steroid reductase deficiency, XY gonadal dysgenesis (Swyer Syndrome), leydig cell hypoplasia, Denys-Drash Syndrome, Smith-Lemli-Opitz Syndrome.

88. Obstetrics And Gynecology Table Of Contents 1085 Treatment for Prolapse of the Sigmoid Neovagina in mayerrokitansky-kuster-HauserSyndrome Among two patients with prolapse of a sigmoid neovagina, one http://www.greenjournal.org/gj11-02b.cfm

TABLE OF CONTENTS Volume / Number 5 (Supplement) November 2002 CASE REPORTS Pelvic Umbrella Pack for Refractory Obstetric Hemorrhage Secondary to Posterior Uterine Rupture The use of a pelvic umbrella pack can be lifesaving in the event of refractory obstetric hemorrhage. Rebecca J. Howard, J. Michael Straughn, Jr, Warner K. Huh, Dwight J. Rouse Shigellosis Complicating Preterm Premature Rupture of Membranes Resulting in Congenital Infection and Preterm Delivery Preterm premature rupture of membranes and congenital acquired infection can be caused by maternal shigellosis. Andrei Rebarber, Brittany Star Hampton, Valerie Lewis, Samuel Bender Dysmenorrhea After Bilateral Tubal Ligation: A Case of Retrograde Menstruation Retrograde menstruation and dilatation of proximal tubal segments with blood after bilateral tubal ligation can cause dysmenorrhea and pelvic pain that mimics the symptoms of endometriosis. Kelly Morrissey, Nadine Idriss, Lynnette Nieman, Craig Winkel, Pamela Stratton Pain in the Foot: Calcaneal Metastasis as the Presenting Feature of Endometrial Cancer Endometrial cancer presenting as a calcaneal metastasis is extremely rare, and aggressive treatment provided effective palliation of symptoms.

89. MEDLINE Abstract TI Congenital absence of the vagina. The mayer-rokitansky-kuster-Hausersyndrome. AU - Griffin JE; Edwards C; Madden JD; Harrod http://www.uptodate.com/patient_info/topicpages/abstrcts/Abstrx10/1017676.htm

TI - Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome. AU - Griffin JE; Edwards C; Madden JD; Harrod MJ; Wilson JD SO - Ann Intern Med 1976 Aug;85(2):224-36 We describe 14 patients with congenital absence of the vagina associated with a variable abnormality of the uterus and review the literature. Associated developmental anomalies of the urinary tract and skeleton are common. As a result of the analysis of two affected families, we believe that the disorder may represent the variable manifestation of a single underlying genetic defect that can be expressed alone or in any combination of vertebral, renal, and genital abnormalities. Some affected persons may have lethal manifestations such as absence of both kidneys, and some cases may result from multifactoral causes rather than a single gene defect. Whatever the cause, the defect involves mesodermal development and the mesonephric kidney, the latter resulting in abnormalities in the paramesonephros (uterus and vagina) and in the metanephric kidney. Both nonoperative and surgical treatments are generally successful in repairing the vaginal abnormality.

90. AnsMe Directory - Health > Conditions And Diseases > M Marburg. Marfan syndrome. MarieSainton Disease. Marinesco-Sjogren syndrome. MayerRokitansky kuster hauser syndrome. McArdle's Disease. Measles, German. Measles,Red. http://dir.ansme.com/health/43355.html

Search: Web Sites Dictionary - Define Dictionary - Sounds Like Dictionary - Relations Dictionary - Rhymes Dictionary - Translate Sponsors Web Directory M Web Directory Health Conditions and Diseases Sub Directories MAC MPS III MRKH Machado-Joseph Disease ... Submit Site All other brands are property of their respective owners. Directory Dictionary AIM Smileys Contact Us

91. Apraxia Resources, From Living With Disabilities Genetic Disorders SourceBook Basic Consumer Information about Hereditary Diseasesand Disorders, Including Cystic Fibrosis, Down syndrome, Hemophil. http://www.pediatricpt.com/disorders/genetic syndromes.htm

Home News Headlines Today's News Headline Archive Daily Living Nutrition Clothing Siblings Toys ... Able Disabled Getting Help Caring for the Caregiver Financial Financing the Future Public Policy and Law ... Disorders More Help Book Store Message Boards About Us About PPT About BBB About Sandra Brooks Legal Notices ... Add to this Site Genetic Syndromes Resources Links to Information about Genetic Syndromes Angelman Syndrome Foundation Asperger Syndrome Coalition of the United States, Inc Association for Repetitive Motion Syndromes CJ Foundation for Sudden Infant Death Syndrome ... Williams Syndrome Association, Inc. NHIC Home Page Books About Genetic Syndromes Genetic Disorders SourceBook: Basic Consumer Information about Hereditary Diseases and Disorders, Including Cystic Fibrosis, Down Syndrome, Hemophil Your Feedback Do you have an experience with a specific disorder that you'd like to share with others or do you need help finding a practical answer to a question about a disorder? Visit

92. Parked Domain - Conexim Australia Domain Name Registration And Web Hosting Servi Genuine Australian web hosting company. Professional hosting, dedicated managed Linux servers, colocation, domain name registration. Apache, PHP, MySQL, PERL, CGI, JSP, SSL, SSI, control panel, email hosting, and custom solutions. http://writtenbyme.com/articleview.php?id=3219

93. ŪªÌQ&A:¤ë¸g¤£¶¶ The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set. http://www.wedar.com/library2/qa-lu1.htm

°ü²£¬ìÂå®v ¿c¤Z ¦^µª: 1 ¤l®c»P³±¹Dªº°ÝD 2 §Z±_ªº°ÝD 3 ¸£¤U««Å骺°ÝD 4 ¤¤¼Ï¯«¸g¨t²Îªº°ÝD ²¤¶¦p¤U: 1 ¤l®c»P³±¹Dªº°ÝD¡G A ¤l®c¤ºªg³s¡G¤SºÙ¡uAsherman's syndrome¡v¡A³q±`»P¤§«eªº¤l®c¤º¤â³N¦³ ö¡A¦p¤H¤u¬y²£¡A¤l®cÂX¨í³N¡A¤l®c¾ã§Î³N¡A¤l®c¦Ù½F¤Á°£³N©Î­å¸¡²£µ¥¡C ¨ä¯S¼x¬O¤ë¸g¶qº¥¶i©Êªº´î¤Ö¡C µ¥µ¥¡C³q±`³y¦¨­ìµo©ÊµL¤ë¸g¡A¶g´Á©Ê¸¡µh¬Æ¦Ü³±¹D¡A¤l®c©Î¸¡µÄ¿n¦å¡C¤ñ ¸û¤Ö¨£ªº¦³¥ý¤Ñ¯Ê¤Ö¤l®c¤º½¤µÄ©Î¤l®c¤º½¤µ¥µ¥¡C a Mayer-Rokitansky-Kuster-Hauser syndrome¡G¦¹¯g­Ô¸s¬°¥¿±`¤k©Ê¦ý¥ý¤Ñ ©ÎÂù¨¤¤l®c¡C¥t¥~±`¦X¨Ö¦³ªc§¿¨t²Î»P°©Àfªº·î§Î¡C b ³±¹D¾î»J c ¸A¤Y¤k©Ê¤Æ¡G¬V¦âÅ鬰¥¿±`¨k©Ê¡]46,XY¡^¡A¦ý¦]¯Ê¤Ö¨k©Ê¶Pº¸»Xªº±µ¨ü¾¹¡A 2 §Z±_ªº°ÝD¡G C ©Ê¸¢¤£µo¥Í¡G¦¹«ü³æ¯Âªº©Ê¸¢¥¼¥Í¦¨¡A¨u¨£¡A­ì¦]¤£©ú¡A¥i¯à»P§³®W¦­´Áªº¯f¬r·P¬V©Î¥NÁ²§±`¦³ö¡C D §Z±_¤£¤ÏÀ³¯g­Ô¸s(Resistent ovarian syndrome)¡G¨u¨£¡A¯f¤HµL¤ë¸g¡AÅ餺ªº ©Ê¸¢¨ë¿E¯À¤Wª@¡A§Z±_¦³Âoªw¡A¬V¦âÅ鬰¥¿±`¤k©Ê(46,XX)¡C F ¦hÅn©Ê§Z±_¡G­ì¦]¤£¬O«Ü²M·¡¡A¥D­n¯S¼x¬°¤ë¸g²§±`¡AªÎ­D»P¨k©Ê¤Æ¡C 3 ¸£¤U««Å骺°ÝD¡G B ªÅµê¾b³¡¯g­Ô¸s(Empty sella syndrome)¡G¥i¯à¬O¥ý¤Ñ©Êªº¯Ê³´©Î¥Ñ©ó¸£¤U««Åé C Sheehan's syndrome¡G±`¦]²£«á¤j¶q¥X¦å©Î¥ð§J¾É­P¸£¤U««Å骺«æ©Êa¦º©Ò­P¡C 4 ¤¤¼Ï¯«¸g¨t²Îªº°ÝD¡G ¦b¤»¦~«á¦Û°Ê«ì´_¥¿±`¡C µù¡GªÎ­D¤]¥i¯à¾É­P¤ë¸g¤£¥¿±`¡A¦ý³q±`¬O]¬°ºC©Êªº¤£±Æ§Z©Ò¤Þ°_¡A»P¤Uµø¥C ªº¤Àªc²§±`¸ûµLö«Y¡C C ¹L«×ªº¹B°Ê¡G¥i¯à»P¯×ªÕ²Õ´¹L¤Ö¡A¤ß²zÀ£¤O¼W¥[¡A¯à¶qÄá¨ú¤£¨¬¦³ö¡A¦P®É¹B°Ê®ÉÅ餺ªº©Ê¸¢¨ë¿E¯À¤Àªc´î¤Ö¡A¦Óªc¨Å¯À¡A¥Íªø¿E¯À¡A¸A¤YଡA¿ËµÇ¤W¸¢¥Ö½è¯À»PµÇ¤W¸¢¯À¤Àªc¼W¥[¡AT3»PT4´î¤Ö¡FEndorphin»P¿ËµÇ¤W¸¢¥Ö½è¯ÀÄÀ©ñ¿E¯Àªº

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