81. Turner Syndrome Information about turner syndrome, which exclusively affects girls, and how human growth hormone therapy can help. http://www.nutropin.com/patient/4_0_about_turner_syndrome.jsp

82. Lilly: Consumers/Patients: Turner Syndrome turner syndrome. turner syndrome. What is turner syndrome? turner syndrome is a condition that affects about one in every 2500 females. http://www.lilly.ca/searchable/cons/turner.htm

Health Centres Osteoporosis Diabetes Mental Health ... Growth Hormone Deficiency Disorder in Children Turner Syndrome Turner Syndrome What is Turner Syndrome? Signs and Symptoms of Turner Syndrome Short stature Ovarian failure Puffy hands or feet at birth Small fingernails or toenails tending to point upwards Small jaw or high arched palate Low set ears Low hairline Webbed neck Pigmented moles Bending out at the elbows History of ear infections History of squinting (strabismus) Short for no apparent reason, or growth slower than expected Failure to begin menstrual periods Lack of sexual maturation

83. Turner Syndrome, Cincinnati Children's Hospital Medical Center turner syndrome genetic abnormalities, features and heart defects information from the Heart Encyclopedia by the Heart Center staff at Cincinnati Children s http://www.cincinnatichildrens.org/health/info/heart/diagnose/turner.htm

Home Contact Us Site Map Go to Advanced Search ... Heart-Related Syndromes Turner Syndrome Noonan Syndrome Down Syndrome Marfan Syndrome Velo-Cardio-Facial Syndrome ... Contact Us Heart-Related Syndromes Turner Syndrome Genetic Abnormality, Features, Heart Defects Explanation Genetic Abnormality Prominent Features Heart Defects What is Turner syndrome? Turner syndrome was initially described by Dr. Henry Turner in 1938. Turner syndrome occurs in approximately 1 of 2,500 females. About 95 percent of fetuses are spontaneously miscarried during pregnancy and thus only 5 percent survive to term. Most cases of Turner syndrome occur randomly and thus do not carry a recurrence risk. Prenatal diagnosis is available through amniocentesis (sampling of the fluid which surrounds the baby before birth) to look for the abnormality of the X chromosome. Since patients with Turner syndrome are unable to have children, there is no risk of mother-daughter transmission. Return to Top Genetic abnormality of Turner syndrome Turner syndrome is characterized by an abnormality in the X chromosome. Normally females have two X chromosomes (and males have one X and one Y). In Turner syndrome, females often have only a single X chromosome. (This occurs in 60 percent of patients with Turner syndrome.)

84. Turner Syndrome Clinic, Cincinnati Children's Hospital Medical Center The turner syndrome Clinic at Cincinnati Children s Hospital Medical Center is a multispecialty clinic for children, adolescents and young adults with http://www.cincinnatichildrens.org/svc/alpha/t/turner-syndrome/

Home Contact Us Site Map Go to Advanced Search ... Turner Syndrome Clinic Overview Faculty and Staff Contact Us Turner Syndrome Clinic Services for Children, Adolescents and Adults with Turner Syndrome The Turner Syndrome Clinic at Cincinnati Children's Hospital Medical Center is a multi-specialty clinic for children, adolescents and young adults with Turner Syndrome (TS) Cincinnati Children's Turner Syndrome Clinic opened during summer 2000. The clinic's staff's goals and objectives are to: Provide comprehensive medical care and health supervision for Turner syndrome patients Offer an integrated approach to the treatment of Turner-syndrome-associated disorders through a multi-specialty team Provide anticipatory guidance and management of learning disorders in Turner syndrome patients Facilitate contact between families of Turner syndrome patients and schools Provide education for families and health care personnel Provide prenatal counseling Cincinnati Children's Turner syndrome Clinic offers information about Turner syndrome support groups , as well.

85. Turner Syndrome,45 X Syndrome,Bonnevie-Ulrich Syndrome,Chromosome turner syndrome,45 X Syndrome,BonnevieUlrich Syndrome,Chromosome X,Monosomy X,Gonadal Dysgenesis 45 X,Gonadal Dysgenesis XO,Monosomy X http://www.icomm.ca/geneinfo/turner.htm

86. Turner Syndrome turner syndrome is a birth defect caused by the absence of an X chromosome in some or all cells of a female, which inhibits sexual development and usually http://www.pennhealth.com/ency/article/000379.htm

87. Medical Genetics - Turner Syndrome turner syndrome is a genetic condition seen in girls that causes them to be shorter Many problems affecting girls with turner syndrome can be managed or http://www.chkd.org/Genetics/turner.asp

88. Vysis: Turner Syndrome Turner s Syndrome is a condition that affects about one in every 2500 females. Unlike females without Turner s syndrome who have two X chromosomes, http://www.vysis.com/TurnerSyndrome_35867.asp

//Set Variables to Use in HM_ScriptDom.js to do conditions on pages var HomePage = false var CartPage = false var CartItem = false var ProductHomePage = false var EditorPage = false var popad = false //Set Variables to Use in HM_ScriptDom.js to do conditions on pages 0 Items in Cart Submitting... Negotiating with host Sending Data Verifying Data Receiving Data PathVysion UroVysion AneuVysion Laboratories ... AneuVysion News //HideChromo and ShowChromo moved to Specific.js 11/28/04 // NOTE: GoToChromosomePage function is located in 02/www/include/Layout/Xsl_Vysis/Javascript so // it can be used globally Turner Syndrome AneuVysion Prenatal Genetic Test Prenatal Testing Genetic Disorders Genetics ... Glossary in vitro fertilization are serving to alleviate many of the problems associated with this condition. For In Vitro Diagnostic Use The AneuVysion Assay (CEP 18, X, Y-alpha satellite, LSI 13 and 21) Multi-color Probe Panel is intended to use CEP 18/X/Y probe to detect alpha satellite sequences in the centromere regions of chromosomes 18, X and Y and LSI 13/21 probe to detect the 13q14 region and the 21q22.13 to 21q22.2 region. The AneuVysion kit is indicated for identifying and enumerating chromosomes 13,18, 21, X and Y via fluorescence in situ hybridization (FISH) in metaphase cells and interphase nuclei obtained from amniotic fluid in subjects with presumed high risk pregnancies. It is not intended to be used as a stand alone assay for making clinical decisions. FISH results are intended to be used as an aid in the diagnosis of numerical abnormalities of chromosomes 13, 18, 21, X and/or Y in conjunction with other information currently used in prenatal diagnosis, consistent with professional standards of practice

89. Turner Syndrome Content is intended for US residents only. turner syndrome / drug therapy; Pharmaceutical Preparations; Patient Education; http://omni.ac.uk/browse/mesh/D014424.html

low graphics Turner Syndrome Turner Syndrome Turner Syndrome / drug therapy Turner Syndrome British Society for Paediatric Endocrinology and Diabetes The British Society for Paediatric Endocrinology and Diabetes (BSPED)has existed since 1979. The society aims "to advance education in paediatric endocrinology and related subjects by promoting research in such areas and disseminating the useful results of such research." The Web site provides information on gland and growth disorders for health professionals, patients and their families. There is a password-protected area for BSPED members. There are also links to professional and patient resources, publications, guidelines, a calendar of BSPED meetings and current/past research projects. Turner Syndrome Societies, Medical Pediatrics Great Britain ... Adrenal Hyperplasia, Congenital Turner Syndrome / drug therapy Humatrope Humatrope is a medication for the treatment of growth hormone deficiency and Turner syndrome, produced by the pharmaceutical company Eli Lilly. Lilly have provided information for patients and health professionals, which includes educational material, resources and a section aimed specifically at children. Content is intended for US residents only. Turner Syndrome / drug therapy Pharmaceutical Preparations Patient Education Last modified: 09 Sep 2005

90. Turner Syndrome turner syndrome is a rare chromosomal disorder of females characterized by short stature and the lack of sexual development at puberty. http://www.bchealthguide.org/kbase/nord/nord112.htm

var hwPrint=1;var hwDocHWID="nord112";var hwDocTitle="Turner Syndrome";var hwRank="1";var hwSectionHWID="nord112-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Turner Syndrome Important It is possible that the main title of the report Turner Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms 45, X Syndrome Bonnevie-Ulrich Syndrome Chromosome X, Monosomy X Gonadal Dysgenesis (45,X) Gonadal Dysgenesis (XO) Monosomy X Morgagni-Turner-Albright Syndrome Ovarian Dwarfism, Turner Type Ovary Aplasia, Turner Type Pterygolymphangiectasia Schereshevkii-Turner Syndrome Turner-Varny Syndrome XO Syndrome Disorder Subdivisions None General Discussion Turner syndrome is a rare chromosomal disorder of females characterized by short stature and the lack of sexual development at puberty. Other physical features may include a short neck with a webbed appearance, heart defects, kidney abnormalities, and/or various other malformations. Among affected females, there is also a heightened incidence of osteoporosis, type II diabetes, and hypothyroidism. There appears to be great variability in the degree to which girls with Turner syndrome are affected by any of its manifestations. Turner syndrome occurs when one of the two X chromosomes normally found in women is missing or incomplete. Although the exact cause of Turner syndrome is not known, it appears to occur as a result of a random error during the division (meiosis) of sex cells.

91. HONselect - Turner Syndrome Translate this page English, turner syndrome, - Bonnevie-Ullrich Syndrome - Gonadal Dysgenesis, 45,X Bonnevie Ullrich Syndrome. Français, Turner, syndrome http://www.hon.ch/HONselect/RareDiseases/C13.371.820.700.842.309.872.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Turner Syndrome - Bonnevie-Ullrich Syndrome - Gonadal Dysgenesis, 45,X - Gonadal Dysgenesis, XO - Status Bonnevie-Ullrich - Turner's Syndrome - Bonnevie Ullrich Syndrome Français: Turner, syndrome Deutsch: Turner-Syndrom - Albright-Turner-Syndrom - Bonnevie-Ullrich-Syndrom - Infantilismus, pterygogonadaler - Ullrich-Turner-Syndrom - Zwergwuchs, ovarieller - Gonadendysgenesie, XO Español: Síndrome de Turner - Síndrome de Bonnevie-Ullrich - Disgenesia Gonadal XO - Disgenesia Gonadal 45 X Português: Síndrome de Turner - Síndrome de Bonnevie-Ullrich - Disgenesia Gonadal XO - Disgenesia Gonadal 45 X HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch Yes Español Yes Português Yes Home About us Site map ... Contact http://www.hon.ch/HONselect/RareDiseases/C13.371.820.700.842.309.872.html Last modified: Wed May 18 2005

92. Turner Syndrome - Bonnevie-Ullrich Syndrome - Information Page With HONselect A syndrome of defective gonadal development in phenotypic women with a karyotype http://www.hon.ch/HONselect/RareDiseases/EN/C13.371.820.700.842.309.872.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Turner Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Turner Syndrome Definition: A syndrome of defective gonadal development in phenotypic women with a karyotype of sex chromosome monosomy (45,X or 45,XO), associated with the loss of a sex chromosome X or Y. Patients generally are of short stature with undifferentiated (streak) gonads, sexual infantilism ( HYPOGONADISM ), webbing of the neck, cubitus valgus, elevated GONADOTROPINS (LH and FOLLICLE STIMULATING HORMONE ) and decreased ESTRADIOL level in blood. Studies of Turner Syndrome and its variants have contributed significantly to the understanding of SEX DIFFERENTIATION NOONAN SYNDROME bears similarity to this disorder; however, it also occurs in males, has normal karyotype, and is inherited as an autosomal dominant. Synonym(s): Bonnevie-Ullrich Syndrome / Gonadal Dysgenesis, 45,X / Gonadal Dysgenesis, XO / Status Bonnevie-Ullrich /

93. Turner Syndrome | Intersex Society Of North America turner syndrome. previous next up. Swyer s Syndrome. What does ISNA recommend for children with intersex? printerfriendly version 149 reads http://www.isna.org/faq/conditions/turner

@import "misc/drupal.css"; @import url(modules/event/event.css); home faq links contact ... agenda Frequently Asked Questions What is intersex? How common is intersex? Intersex conditions How do I know if I have an intersex condition? ... Who was David Reimer (also, sadly, known as "John/Joan")? Our Supporters Arcus Foundation The California Endowment Gill Foundation Kicking Assets Small Change Foundation Over 1,000 individual supporters like you Sections About Board Members Emeritus Funders ... Recent Publications Featured Research Agonize, then Cut this way! Effects of Clitoral Surgery Better Browsing! Home Turner Syndrome previous next up What does ISNA recommend for children with intersex? printer-friendly version Building a world free of shame, secrecy, and unwanted sexual surgeries since 1993 Get ISNA News Get the Video! Upcoming events (event) (7 days) Cheryl Chase at Gay and Lesbian Medical Association Annual Conference (event) (13 days) (event) (68 days) Intersex Activists present keynote at RWJ Human Sexuality Course (event) (115 days) First World Congress on Gender-Specific Medicine (event) (166 days) Nina Williams moderates panel at New Jersey Psychological Association (event) (231 days) more Contact ISNA Detailed contact info Who's online There are currently users and 21 guests online.

94. Hill Health Topics A-Z - Turner Syndrome turner syndrome occurs when one of the two X chromosomes normally found in women Although the exact cause of turner syndrome is not known, it appears to http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord112&SE

95. Turner's Syndrome Hi Brian turner syndrome is a chromosomal condition that results from the total In turner syndrome, the child inherits one X chromosome from one parent, http://www.newton.dep.anl.gov/askasci/bio99/bio99590.htm

Ask A Scientist Biology Archive Turner's Syndrome Back to Biology Ask A Scientist Index NEWTON Homepage Ask A Question ... NEWTON is an electronic community for Science, Math, and Computer Science K-12 Educators. Argonne National Laboratory, Division of Educational Programs, Harold Myron, Ph.D., Division Director.

96. Turner Syndrome - Lucile Packard Children's Hospital turner syndrome is a genetic disorder seen in girls that causes them to be shorter Many problems affecting girls with turner syndrome can be managed or http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/genetics/turner.html

Genetics Clinic Metabolic/Biochemical Genetics Clinic Medical Geneticists Medical Genetics ... Packard Children’s Hospital Pediatrician Receives E. Mead Johnson Award For Pediatric Research Medical Genetics Turner Syndrome What are monosomies? The term monosomy is used to describe the absence of one member of a pair of chromosomes. Therefore, there is a total of 45 chromosomes in each cell of the body, rather than 46. For example, if a baby is born with only one X sex chromosome, rather than the usual pair (either two X's or one X and one Y sex chromosome), the baby would be said to have "monosomy X." Monosomy X is also known as Turner syndrome. What is Turner syndrome? Turner syndrome is a genetic disorder seen in girls that causes them to be shorter than others and to not mature sexually as they grow into adulthood. The severity of these problems varies among affected individuals. Other health problems may also be present involving the heart or renal system (i.e., kidneys). Many problems affecting girls with Turner syndrome can be managed or corrected with appropriate medical treatment. Turner syndrome occurs in one in 2,500 females born. The name "Turner syndrome" comes from the physician, Dr. Henry Turner, who first described the collection of findings in 1938. It was not until 1959 that the cause of Turner syndrome (having only a single X chromosome) was identified.

97. Turner Syndrome a CHORUS notecard document about turner syndrome. turner syndrome. 45 XO female (or mosaic XO/XX) incidence 12500 liveborn females http://chorus.rad.mcw.edu/doc/00406.html

CHORUS Collaborative Hypertext of Radiology Multisystem entities About CHORUS Search Feedback Turner syndrome 45 XO female (or mosaic XO/XX) incidence 1:2500 liveborn females short stature, delayed skeletal maturation osteoporosis short 4th + 5th metacarpals broad, "shield" chest cardiovascular anomalies: present in 20% 70% are coarctation ovarian dysgenesis kidneys: horseshoe kidney, bifid renal pelvis cystic hygroma Charles E. Kahn, Jr., MD - 2 February 1995 Last updated 26 May 2004 Related CHORUS documents: cystic lymphangioma short metacarpals Huntington disease (chorea-athetosis) agenesis of corpus callosum ... scaphoid (navicular) fracture Search for related articles: AJR American Journal of Roentgenology PubMed : index to biomedical literature ... Medical College of Wisconsin

98. Turner's Syndrome Society, Texas Providing links and information about turner's syndrome. Definition and Synonyms, FAQ, TSS Societies (National, State, and Local), Associated Links, Newsgroup discussions, Conference Information. http://www.onr.com/ts-texas/

99. The Turner Center Literature on XYY, Klinefelter, XXX, and turner's syndrome. http://www.aaa.dk/turner/engelsk/

The Turner Center Center for Information, Councelling and Research on chromosome anomalies. Danish Edition German Edition Psychiatric Hospital Aarhus Skovagervej 2 DK-8240 Risskov Denmark Telephone: +45 77 89 36 09 Fax: +45 77 89 30 99 e-mail The Turner Center French Edition New: All our booklets are now available online. Printed copies of these booklets are available free of charge - by request of persons, or parents to persons, afflicted by one of these syndromes. However, we encourage people with access to the Internet to use this option, in order to save overseas postage. Turner's Syndrome: Brief Information In the danish version two litterature lists are included Links to these are added below. Note: Not all texts are in english. List 1 List 2 Booklet on Estrogen Treatment of Turner's Syndrom. Book on Turner's Syndrome Klinefelter Syndrome: Brief Information Literature on Klinefelter's Syndrome Booklet on Klinefelter's Syndrome XYY Syndrome: Brief Information Literature List Booklet on XYY Syndrome Triple-X Syndrome: Brief Information Triple X Literature Booklet on Triple-X Syndrome Follow-up of 25 unselected children with sex chromosome abnormalities to age 12: Brief Information Article on Follow-up Follow-up 20 years later of 34 Klinefelter males with karyotype 47,XXY and 16 hypogonadal males

100. AGAT/Ce Site Et L'association Ont Pour But Principal D'aider Les Personnes, Qui Fournit de l'aide et des informations sur le syndrome de turner. Liste des centres r©gionaux. Paris, France. http://www.agat-turner.org

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