Extractions: Text Size A A A Front Page ... Chromosomal : WAGR Syndrome UF Scientist Finds Unexpected Link Between Cat And Human AIDS Viruses (September 9, 2005) full story Mayo Clinic Develops New Coma Measurement System (September 8, 2005) full story Nitric Oxide Could Extend Fertility (September 8, 2005) Biochemistry , an American Chemical Society journal. full story Flipped, Expelled, Copied, And Shrunk: Researchers Document Dramatic Genome Alterations During Primate Evolution (September 6, 2005) Genome Research presents a series of studies that provide insight into the evolution and variation of primate genomes. The issue will appear online and in print on September 1, concomitant with the publication of the chimpanzee genome sequence in the journal Nature full story Discovery Will Aid Identification Of Misregulated Genes In Rett Syndrome (September 4, 2005)
Aniridia Network International - Aniridia Directory wagr syndrome. Also see Wilms tumour. emedicine.com wagr syndrome wagr syndrome.National Library of Medicine - WAGR -USA http://www.aniridia.org/directory/WAGR.html
Extractions: Supporting people with aniridia and their Families Just Diagnosed? click here Homepage About Us About Aniridia ... Make a Donation Web www.aniridia.org Also see Wilms tumour emedicine.com - WAGR syndrome WAGR Syndrome National Library of Medicine - WAGR -USA Human Genome Mapping Project - WAGR - UK National Library of Medicine - Chromesome 11pdel. syndrome -USA Atlas of Genetics and Cytogenetics in Oncology and Haematology WAGR WAGR in finnish Have a website you would like to add? Submit your URL to Hannah@aniridia-network.net
WAGR References Submicroscopic Deletions At The WAGR Locus PMID 2570677, UI 89377247 Aniridia as part of a wagr syndrome in a girl whosebrother presented wagr syndrome www.bashour.com/examprep/documents/ http://www.aniridia.org/conditions/WAGR.txt
Extractions: WAGR References Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization. Fantes JA, Bickmore WA, Fletcher JM, Ballesta F, Hanson IM, van Heyningen V MRC Human Genetics Unit, Western General Hospital, Edinburgh, United Kingdom. PMID: 1334370, UI: 93098243 Cytogenet Cell Genet 1989;50(2-3):70-4 Molecular definition of de novo and genetically transmitted WAGR- associated rearrangements of 11p13. Lavedan C, Barichard F, Azoulay M, Couillin P, Molina Gomez D, Nicolas H, Quack B, Rethore MO, Noel B, Junien C Institut National de la Sante et de la Recherche Medicale, Unite 73, Paris, France. PMID: 2570677, UI: 89377247 Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias. Lorda-Sanchez I, Sanz R, Diaz-Guillen MA, Fernandez-Toral J, Heine-Suner D, Rodriguez De Alba M, Gonzalez-Gonzalez C, Trujillo MJ, Ramos C, Rodriguez De Cordoba S, Ayuso C. Departmento de Genetica, Fundacion Jimenez-Diaz, Madrid, Spain. ilorda@fjd.es R. Muto1,3, S. Yamamori2, M. Osawa1, H. Ohashi3. 1) Department of Pediatrics, Tokyo Womens Med. Univ., Shinjuku-ku, Tokyo Japan; 2) Research department Mitsubishi Kagaku Bio-Clinical Laboratories, Inc.Tokyo Japan; 3) Division of Medical Genetics, Saitama Children's Medical Center, Saitama Japan. WAGR Syndrome www.bashour.com/examprep/documents/ GLAUCOMA%20Oral%20Questions.pdf The predictive value of FISH analyses for possible occurrence of Wilms tumor in aniridia patients with/without chromosome abnormalities around 11p13. R. Muto1,3, S. Yamamori2, M. Osawa1, H. Ohashi3. 1) Department of Pediatrics, Tokyo Womens Med. Univ., Shinjuku-ku, Tokyo Japan; 2) Research department Mitsubishi Kagaku Bio-Clinical Laboratories, Inc.Tokyo Japan; 3) Division of Medical Genetics, Saitama Children's Medical Center, Saitama Japan.
HighWire -- Browse Journals - WAGR Syndrome Browse Journals publishing on wagr syndrome, (return to Topic List page) Alphabet, , Frequency of articles in wagr syndrome, , Focus of journal on http://highwire.stanford.edu/lists/topic_dir/608683/618131/622317/622443/622456/
Extractions: Sort by: Alphabet Frequency of articles in WAGR Syndrome Focus of journal on WAGR Syndrome What's this? Journals focusing on WAGR Syndrome (in order by highest focus) Pediatric Research info free ISSUES Cancer Research ... Urogenital Abnormalities WAGR Syndrome Home Adv. Search For Institutions For Publishers ... partners/suppliers
HighWire -- Browse Journals - WAGR Syndrome Orthoguide.com wagr syndromeSearch AltaVista for wagr syndrome Global Search Add Url - Free Medline -Contact Us - Search. Enter Keywords to Search and Your Choice of Search http://highwire.stanford.edu/lists/topic_dir/608683/608684/614552/614553/614679/
Extractions: Sort by: Alphabet Frequency of articles in WAGR Syndrome Focus of journal on WAGR Syndrome What's this? Journals focusing on WAGR Syndrome (in order by highest focus) Pediatric Research info free ISSUES Cancer Research ... Urogenital Abnormalities WAGR Syndrome Home Adv. Search For Institutions For Publishers ... partners/suppliers
Extractions: @import "/ng/style.css"; NATURE.COM NEWS@NATURE.COM NATUREJOBS NATUREEVENTS ... Help E-MAIL: PASSWORD: Save password Forgotten password? SEARCH JOURNAL Advanced search Journal home Archive Table of Contents ... For librarians NPG Resources Nature Nature Cell Biology Nature Medicine Nature Reviews Genetics ... Browse all publications Correspondence Nature Genetics doi:10.1038/ng0994-13a Vicki Huff Department of Experimental Pediatrics, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA REFERENCES Jinno, Y. et al Nature Genet. Article PubMed ISI ChemPort Huff, V. et al Am. J. hum. Genet. PubMed ISI ChemPort Riccardi, V.M. et al Pediatrics PubMed ISI ChemPort Franke, U. et al Cytogenet. cell Genet. PubMed Riccardi, V.M. et al J. Pediatr. PubMed ISI ChemPort Riccardi, V.M. et al Cancer Genet. Cytogenet. Article ISI Compton, D.A. et al Cell Article PubMed ISI ChemPort Huff, V. et al Am. J. hum. Genet. PubMed ISI ChemPort Lavedan, C. et al Cytogenet. cell Genet. PubMed ISI ChemPort J. Pediatr. PubMed ISI ChemPort J. Pediatr.
Accessing Article wagr syndrome is a rare contiguous gene disorder characterized by Wilms tumor, A 25year-old girl with wagr syndrome was referred to the ophthalmology http://www.nature.com/ejhg/journal/v13/n4/full/5201358a.html
Extractions: Most users gain access to full text articles through a site license. This is available to institutional customers only. For further information visit the Librarian Gateway. Full-text articles are also available through a number of other options: I want to purchase this article Select this option to view this article immediately and access it for seven days. I am already a personal subscriber to European Journal of Human Genetics Personal subscribers to European Journal of Human Genetics can view this article. To do this you need to associate your subscription with your registration via the My Account page. If you already have an active online subscription, log in via the login box in the top right-hand corner of this page.
Our Story - Reaching Out Network I was told that Nicholas was born with what doctors call wagr syndrome, resultingfrom a deletion of the 11th chromosome. I was not prepared for what I was http://members.aol.com/TheMooZoo/
Extractions: Shortly after birth his doctors informed us that he had undescended testicles. Before leaving the hospital Nicholas was seen by a urologist. The urologist had told us undescended testicles was a common condition in boys. We were still a little scared and concerned. We had hoped his testes would eventually drop down, as they often do in many cases. We made arrangements for a follow up meeting with him 10 days later. We received a call from our pediatricians office about a week later. We were told that a blood test revealed a problem with one of Nicholas' chromosomes. The doctor did not go into much details. He did recommend that we meet with someone in genetics. We were more scared, confused and in need of some answers. It was at the follow up appointment with urology that everything became much clearer, or much more vague, depending how you look at things. I took Nicholas to the appointment alone. I was told that Nicholas was born with what doctors call WAGR Syndrome, resulting from a deletion of the 11th chromosome. I was not prepared for what I was about to hear. His doctor spoke about a kidney tumor, a visual impairment, possible retardation and so much more. Nicholas was crying and my heart was breaking inside. I barely had enough strength or composure to drive home from the doctor's office.
Geneticalliance.org wagr syndrome Support Groups Reaching Out WAGR/Aniridia Network 2063 ReginaLincoln Park, MI 48146 Phone 313.381.4302 http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t
Birth Disorder Information Directory - W Aniridia-Genitourinary Anomalies-Mental Retardation (WAGR) Syndrome/Triad.wagr syndrome chromosome 11p deletion syndrome GENITOURINARY DYSPLASIA http://www.bdid.com/defectw.htm
Extractions: HOME W Syndrome Waaler Aarskog Syndrome (Hydrocephalus with Costovertebral Dysplasia and Sprengel Anomaly) Waardenburg Syndrome -Shah Syndrome with Hirschsprung Disease Wagner Syndrome (Erosive Vitreoretinopathy, Hyaloideoretinal Degeneration of Wagner, Wagner Vitreoretinal Degeneration) Wagner-Stickler Syndrome WAGR Syndrome Walbaum Titran Durieux Crepin Syndrome (Fibular Hypoplasia with Scapulo Pelvic Dysplasia and Absent 5th Fingers) Walker Dyson Syndrome (Aniridia-Mental Retardation Syndrome) Walker Warburg Syndrome (Cerebroocular Dysgenesis; Cerebroocular Dysplasia-Muscular Dystrophy Syndrome; Chemke Syndrome; COD-MD Syndrome; Hard +/- E Syndrome; H ydrocephalus
Extractions: maladies de l'appareil génital féminin et complications de la grossesse maladies de l'oeil maladies du système nerveux maladies et malformations congénitales, héréditaires et néonatales ... tumeurs Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources : Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; informations sur la pathologie, signes de la maladie, autres sites internet, types de consultation adaptées, laboratoires de diagnostic, association de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2002 ; visité le : 13/08/2003].
APSA :: For Parents: Wilmsâ Tumor wagr syndrome (lack of an iris, genitourinary abnormalities, mental retardation).Hemihypertrophy (enlarged body parts on one side) http://www.eapsa.org/parents/wilms.htm
Extractions: The tumor also rarely may be a site of erythropoietin production which is the hormone responsible for increasing the number of red blood cells in the blood stream. Laboratory tests are usually otherwise normal except in rare instances in which the bleeding and clotting tests are normal. Diagnostic Evaluation The next diagnostic test obtained is a computed tomography (CT) scan of the abdomen. (See Figure 1). CT scan shows the tumor within the kidney, often with a rim of normal kidney tissue around the edge and distortion of the urine collecting system of the kidney and displacement of the kidney toward the center of the body. A chest CT is obtained to evaluate for the presence of tumor spread to the lungs. These studies detect the most common sites of tumor spread: lymph nodes, lung, and liver. A CT scan cannot determine whether the tumor can be removed, however, because this can be assessed accurately only at the time of surgery.
ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page MALADIE wagr syndrome. Synonyme(s) Aniridie - tumeur de Wilms. CIM Q87.8.Le syndrome de WAGR (Wilms tumor-Aniridia-Genitourinary anomalies -mental http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=893
WAGR Syndrome Translate this page Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/FR/wagr_syndrome.html
Extractions: Le syndrome de WAGR (Wilms tumor-Aniridia-Genitourinary anomalies -mental Retardation) associe une prédisposition à la tumeur de Wilms survenant à un âge variable, une aniridie totale ou partielle pouvant être associée à une cataracte ou un glaucome, un retard mental variable et des anomalies génitales variant de l'ambiguïté sexuelle à l'ectopie testiculaire associée à des anomalies urinaires. Ce syndrome est dû à une microdélétion de la région chromosomique 11p13. Cette délétion apparaît de novo dans la majorité des cas mais peut être héritée par transmission d'une translocation parentale. *Auteur : Equipe Editoriale d'Orphanet (septembre 2002)*. Signes de la maladie Mise à jour : 04/09/2005 Accès à la base de données Orphanet
Brusa-Torricelli Syndrome (www.whonamedit.com) Since the early 1980s this disorder has commonly been referred to as wagr syndrome.We thank Kelly Trout of the International wagr syndrome Association for http://www.whonamedit.com/synd.cfm/2404.html
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A congenital syndrome in which aniridia (congenital absence of the iris) and nephroblastoma (Wilms' tumour) is associated with mental retardation, craniofacial defects (microcephaly), growth retardation and skeletal anomalies, deformed pinna, genitourinary anomalies, hamartomas, and umbilical and inguinal hernias. Other frequent features include cataract and glycoma, hypospadias, hemihypertrophy, and horseshoe kidney. The syndrome affects both sexes but is more frequent in males. Since the early 1980s this disorder has commonly been referred to as WAGR syndrome.
Principal's Office: Welcome (University Of Dundee) Another similar disease is the wagr syndrome, but rather than point mutation we have We have developed two transgenic models of DDS and wagr syndrome, http://www.dundee.ac.uk/principalsoffice/discoverydays2004/fleming.html
Extractions: Another similar disease is the WAGR syndrome, but rather than point mutation we have found that this is a contiguous gene syndrome, involving loss of extensive chromosomal material on chromosome 11 including the WT1 gene, resulting in a constitutional loss of one copy of WT1. Recently it has been shown that 38% of WAGR patients subsequently develop renal failure. In both, DDS and WAGR disease develops despite possession of one normal copy of WT1, although the rate of progress and precise nature of the disease differs between the two syndromes. We subsequently found that, in both syndromes, the development of a Wilms' tumour requires a second event at WT1, usually loss of the one remaining normal allele (gene). Transgenic models of WT1 associated disease
Extractions: Search for: Limit by: All Topics Original Reports Review Articles Special Articles Biology of Neoplasia Editorials Comments and Controversies Diagnosis in Oncology Art of Oncology Correspondence All Years Browse by Topic or Issue Home Search/Browse Subscriptions ... Customer Service This Article Full Text Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a colleague Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Breslow, N. E. Articles by Nichols, K. E. Journal of Clinical Oncology , Vol 21, Issue 24 (December), 2003: 4579-4585
Extractions: Search for: Limit by: All Topics Original Reports Review Articles Special Articles Biology of Neoplasia Editorials Comments and Controversies Diagnosis in Oncology Art of Oncology Correspondence All Years Browse by Topic or Issue Home Search/Browse Subscriptions ... Customer Service This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a colleague Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Breslow, N. E. Articles by Nichols, K. E. Journal of Clinical Oncology , Vol 21, Issue 24 (December), 2003: 4579-4585
