61. Select Entries From OMIM -aniridia 106210 PAIRED BOX GENE 6; PAX6 106200 ANIRIDIA; AN1 *206700 ANIRIDIA, CEREBELLARATAXIA, AND MENTAL DEFICIENCY 194072 wagr syndrome 106220 ANIRIDIA AND http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/eye/aniridia.htm

Select Entries from OMIM Online Mendelian Inheritance in Man Back to Senses Abnormalities 33 entries found, searching for "aniridia" PAIRED BOX GENE 6; PAX6 ANIRIDIA; AN1 ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY WAGR SYNDROME ANIRIDIA AND ABSENT PATELLA ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION WILMS TUMOR 1; WT1 CATALASE; CAT GENITOURINARY DYSPLASIA COMPONENT OF WAGR SYNDROME; GUD V-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB PHEOCHROMOCYTOMA LETHAL ANTIGENA1; AL-A1 KERATITIS, HEREDITARY MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA ECTOPIA PUPILLAE FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROME ANTIGEN DEFINED BY MONOCLONAL ANTIBODY F10.44.2 CAT EYE SYNDROME; CES HALLERMANN-STREIFF SYNDROME; HSS LACTIC ACIDURIA DUE TO D-LACTIC ACID NEUROBLASTOMA STAGE 4S GENE PETERS ANOMALY WITH CATARACT SYNDECAN 2; SDC2 EXOSTOSES, MULTIPLE, TYPE II SUPPRESSOR OF TUMORIGENICITY 2; ST2

62. Children's Memorial Hospital (Chicago, IL) -- Center For Cancer & Blood Diseases A small percentage of patients with Wilm's tumor have one of threegenetic syndromes, including the following wagr syndrome. The http://www.childrensmemorial.org/depts/cancer/wilms1.asp

Home Medical Departments Hematology/Oncology Wilm's Tumor What is Wilm's tumor? What causes Wilm's tumor? What are the symptoms of Wilm's tumor? What is Wilm's tumor? Wilm's tumor, also called nephroblastoma, is a malignant (cancerous) tumor originating in the cells of the kidney. It is the most common type of renal (kidney) cancer and accounts for about 6 percent of all childhood cancers. Approximately 400 children in the US are diagnosed with a Wilm's tumor each year. The disease can occur at any age between infancy and 15 years, but, in most cases, the tumor is detected by the age of 3. This cancer affects males and females equally. The tumor can be very large and it may spread (metastasize) to other body tissues. The most common site for Wilm's tumor to metastasize is the lungs. Lesions may also occur, however, in the liver, the other kidney, brain, and/or bones. In approximately 5 to 10 percent of children with Wilm's tumor, both kidneys are involved. Other tumors such as rhabdoid tumors of the kidney, clear cell sarcoma of the kidney, and mesoblastic nephroma occur in the kidney but are not Wilm's tumors and have different prognoses and treatment. Return to top What causes Wilm's tumor?

63. Wilms Tumor, Cincinnati Childrens Hospital Medical Center wagr syndrome WAGR stands for the four diseases present in this syndrome, includingWilms tumor, aniridia (absence of the iris, which is the colored part http://www.cincinnatichildrens.org/Health_Topics/Your_Childs_Health/Cancer/Condi

Your Child's Health Cancer Conditions and Diagnoses Hepatoblastoma ... Rhabdomyosarcoma Wilms Tumor Home Care Overview Wellness Conditions and Diagnoses Wilms Tumor What is Wilms tumor? Wilms tumor, also called nephroblastoma, is a malignant (cancerous) tumor that originates in the cells of the kidney. It is the most common type of kidney cancer in childhood, affecting males and females equally and accounting for about 6 percent of all pediatric cancers. Approximately 500 children in the United States are diagnosed with this tumor each year. Although the disease can occur at any age between infancy and 15 years, it is generally detected by age 3. The tumor can be very large and it may metastasize (spread) to other body tissues. The most common site of spread is the lungs, but lesions may also occur in the other kidney, the brain, and/or bones. In approximately 5 to 10 percent of children with Wilms tumor, both kidneys are involved. Treatment strategies depend on a number of factors, including the stage of the disease and the microscopic pathology of the tumor. However, surgical removal of the tumor is the cornerstone of therapy. Collaborative treatment strategies that involve pediatric surgeons, pediatric oncologists (cancer specialists), and radiation oncologists have resulted in cure rates that exceed 90 percent.

64. CancerGene WT1 Class, GATEKEEPER; TRANSLOC; TUMORSUPPRESSOR. Diseases, Kidney Neoplasms;Nephroblastoma; wagr syndrome. 607102, Link to 194072, wagr syndrome, (3). http://caroll.vjf.cnrs.fr/cancergene/CG199.html

Infobiogen Search CancerGene CancerGene Homepage Search CancerGene Citations CancerGene Card Symbol Aliases GUD; WAGR; WIT-2 Name Wilms tumor 1 Locus OMIM GDB SwissProt LocusLink Atlas of Genetics and Cytogenetics in Oncology and Haematology : Class GATEKEEPER; TRANSLOC; TUMOR-SUPPRESSOR Diseases Kidney Neoplasms; Nephroblastoma; WAGR Syndrome Note WT1 gene is fused to EWS ( CG:36 ) in t(11;22)(p13;q12) in desmoplastic small round cell tumor (DSRCT) ( UI:95166761 ). Lee et al. (1997, UI:98016415 ) concluded that the oncogenic fusion of EWS to WT1 in DSRCT results in the induction of PDGFA ( CG:403 ) , a potent fibroblast growth factor that contributes to the characteristic reactive fibrosis associated with this unique tumour. Identification of WTAP( CG:1423 ), a novel Wilms' tumour 1-associating protein by Little et al. (2000, UI:20458888 Comments Johnstone et al. (1996, UI:97098673 ) showed that WT1 and par-4 (prostate apoptosis response protein 4; CG:1034 ) interact specifically both in vitro and in vivo and that this interaction is mediated by the zinc fingers of WT1 and the leucine repeats of par-4. Functional analyses showed that par-4 inhibited transcription activated by WT1 and augmented WT1-mediated transcriptional repression. WT1 encodes a zinc finger transcription factor implicated in kidney differentiation and tumorigenesis. In reporter assays, WT1 represses transcription from GC- and TC-rich promoters, but its physiological targets remain uncertain. Lee et al. (1999

65. ACS :: What Are The Risk Factors For Wilms' Tumor? syndrome. In the wagr syndrome the same gene (the gene on chromosome11) may be partially or completely deleted in all body cells. In http://www.cancer.org/docroot/CRI/content/CRI_2_4_2X_What_are_the_risk_factors_f

66. AtObGyn: Obstetrics And Gynecology Search Engine 1998 © NLM) Mixed Gonadal Dysgenesis Turner's Syndrome - Hermaphroditism - Pseudohermaphroditism- Kallmann Syndrome - wagr syndrome - Urogenital Neoplasms http://www.atobgyn.com/obgyn/index2.php3

Global Search Add Url Free Medline Contact Us ... Conferences Bookmark this page for your Future Medline/Internet Searches Try the Medline Search Designed for ObGyn With FAST results ObGyn Internet Search Medline Search Designed for ObGyn Enter Keyword to search help Or And Match entire phrase Enter Keyword to search help Common Terminology General ObGyn (MESH 1998 © NLM) Adnexal Diseases Adnexitis Oophoritis ... XY Gonadal Dysgenesis 46 General ObGyn (MESH 1998 © NLM) Mixed Gonadal Dysgenesis Turner's Syndrome Hermaphroditism ... ObGyn

67. Results Of The Search Your submitted paragraph wagr syndrome A CONTIGUOUS GENE SYNDROME characterizedby the association of WILMS' TUMOUR (a childhood nephroblastoma) with Aniridia http://chaos.swmed.edu/etblast/user/user-1015659130/lforem.html

eTBLAST Statistics Summary Your submitted paragraph The eTBLAST analysis that you have requested was successful. The closest matches are shown below. Abstracts of the Nordic Symposium: Mental Retardation in Childhood. Oslo, February 13-15, 1992. Genet Couns 1992;3(3):161-71. Evidence for visual imagery deficits in persons with mental retardation. Courbois Y Am J Ment Retard 1996 Sep;101(2):130-48. Aniridia-Wilms' tumour syndromea case report. Vidyasagar MS ... Rao P Indian J Ophthalmol 1992 Oct-Dec;40(4):122-3. General slowing of information-processing by persons with mental retardation. Kail R Am J Ment Retard 1992 Nov;97(3):333-41. Development of a theory of mind in individuals with mental retardation. Benson G ... Maas F Am J Ment Retard 1993 Nov;98(3):427-33. Mental retardation research in the Soviet Union. Holowinsky IZ Ment Retard 1990 Aug;28(4):211-8. Research in mental retardation: toward an etiologic approach. Dykens EM ... Hodapp RM J Child Psychol Psychiatry 2001 Jan;42(1):49-71. Is outerdirectedness employed in a harmful or beneficial manner by students with and without mental retardation? Bybee J ... Zigler E Am J Ment Retard 1992 Mar;96(5):512-21.

68. WAGR Wheels Support Site WAGR WHEELS is a website for families affectedby wagr syndrome and related conditions.OurGoal is to link families to sources of information, to support, and http://www.angelfire.com/ga3/wagr/

WAGR Wheels Support Site What does Wheels mean? W agr H E xcellence in E ducation L ove S haring WAGR WHEELS is a website for families affectedby WAGR Syndrome and related conditions.Our Goal is to link families to sources of information, to support, and to one another. WAGR Links We have an email discussion group! "Reaching Out" The WAGR/Aniridia Networknewsletter CFAR, The Canadian Foundation for Aniridia Research Parenting a Child or Young Adult with a Disability ... National Kidney Foundation Email: 2fish@surfsouth.com Page By Mad Jim Hall

69. Untitled otorenal syndrome Frasier syndrome renal dysplasia Simpson–Golabi–Behmelsyndrome Townes–Brocks syndrome wagr syndrome FURTHER INFORMATION http://www.nature.com/cgi-taf/DynaPage.taf?file=/nrg/journal/v3/n7/links/nrg842_

70. Health Library The results of your search for W are Waardenburg Syndrome. wagr syndrome.Waldenstrom's Macroglobulinemia. Waldmann Disease. Walker Warburg Syndrome. http://www.ochsner.org/library/healthguide/IllnessConditions/_SearchResults.asp?

71. Gene WT1ID78 affecting zinc fingers in exons 710. (wagr syndrome, genito-urinary(GU) anomalies, Denys-Drash-syndrome, Frasier syndrome; see below). http://www.infobiogen.fr/services/chromcancer/Genes/WT1ID78.html

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumours ... Wilms' tumor Disease nephroblastoma of childhood Prognosis good with treatment according to NWTS or SIOP Cytogenetics 11p13 deletions/translocations can be seen in some cases Oncogenesis up to 15% of tumors show mainly biallelic inactivation of WT1 through deletion or mutatio Entity desmoplastic small round cell tumor (DSRCT) Prognosis poor Cytogenetics translocations, t(11;22)(p13;q12) Abnormal Protein With EWS : EWS-WT; in frame fusion of EWS exons 1-7 and WT1 exons 8-10 Entity Denys-Drash syndrome (DDS) Disease defined by: mesangial sclerosis with kidney failure (age 2 yrs), gonadal dysgenesis, risk of Wilms' tumors Prognosis kidney failure at age 0-5 years Hybrid/Mutated Gene dominant negative mutations, especially missense mutations within the zinc fingers (aa 394 Arg -> Trp) but very few nonsense mutations Oncogenesis high risk of Wilms' tumor development Entity Frasier syndrome Disease defined by: complete gonadal dysgenesis, focal glomerular sclerosis, gonadoblastoma; in karyotypic females the syndrome may be limited to focal glomerular sclerosis with regular gonadal development and function Prognosis kidney failure at age 10-30 years Hybrid/Mutated Gene heterozygous point mutations of alternative splice donor site in exon 9 with imbalance of WT1 isoform ratio Oncogenesis gonadoblatoma may occur within streak gonads External links Hugo Genes Cyto Gene Seq [Map View - NCBI] GeneCards CancerGene GDB Genatlas ... Genbank [ SRS ]

72. Links: Health: Rare Disorders- Alabama Council For Developmental Disabilities Syndrome; Tyrosinemia; Usher Syndrome; VATER Syndrome; VeloCardio-FacialSyndrome; Waardenburg Syndrome; wagr syndrome; Weaver Syndrome; http://www.acdd.org/Links/conditions/Rare_Disorders.htm

You are here: Home Links Conditions Rare Disorders Rare Disorders Home About Definition Planning ... Search On this page: General Disorders General Cherubs - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family - Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrous Dysplasia Support Online - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation - Information about growth-related disorders through education, research, and advocacy. Member driven organization. International Rare Disease Support Network - A community providing more than a 1000 different links to support groups for the people of all nations. Kindler Syndrome - An article and case study of this rare disease. Includes links. National Organization for Rare Disorders, Inc.

73. Resource Links Section 2 Chromosome Deletion Outreach, Inc. (CDO) Rare Chromosom Chromosome 11 Deletion/wagr syndrome Support Group C/O Anne Prusakiewicz 2063 ReginaLincoln Park, MI 48146 Email ReachingOutNet@aol.com HomepageChromosome http://www.chromodisorder.org/support2.htm

About CDO Contact Us Join CDO Donate ... Volunteer Select a Page More about Chromosome Deletion Outreach Registered Chromosome Disorders CDO Family Stories Intro to Chromosome Abnormalities Ask the Doctor Library Resources Secure Application Form CDO Angels NICU Stories Guestbook T-Shirts FAQS Inspirational Chromosome Deletion Outreach, Inc. Related Resource Information Additional Listings This information is not intended as an endorsement or recommendation of any organization - it is intended for informational and educational purposes only. Always check with your healthcare provider should you have any questions or concerns. CDO's Inspirational Page Website: http://home.attbi.com/~sdel67/ Angelman Syndrome Website: www.angelman.org Chromosome 3 Registry - Online Information Website: Chromosome 3 Registry 4p- Support Group 2585 Taylor Longview WA 98632 EMail: syork@scattercreek.com Website: www.4p-supportgroup.org Priority 4 Families - Chromosome 4 Disorder Support Brenda Grimmett 5536 Virginia Ct Amherst, OH 44001 440-282-1460 ph 440-989-2005 fax EMail: bgrimmett@eriecoast.com

74. Search By Disease 14 wagr syndrome. 15 WardRomano syndrome (WRS). Should you not find the diseasefor which you are searching, please send an email to EDDNAL eddnal@skypro.be. http://www.eddnal.com/directory/disease.php?letter=W

75. MUMS List Of Disorders - U - Z Disease (5) *. WSyndrome (1); wagr syndrome (Wilms Tumor-Aniridia-GonadoblastomaM.lR.) (8) *; Waardenburg Syndrome (6); Waardenburg http://www.netnet.net/mums/mum_u-z.htm

Return to MUMS Home Page MUMS: List of Disorders U - Z Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. UPJ Obstruction (4) Uhl Anomaly (Ventricular myocardium, aplasia of right) (1) Ulcerated Colitis (4)* Ulna Bone, absence, bilateral (arm bone) (3) * Ulna Bone, deficiency (arm bone) (4) * Undescended Testes (72) Undiagnosed (498) Unusual Facies Syndrome (5) Ureathra, Diverticulum (1) Ureter Reconstruction (5) Ureterostomy (5) Urethra Fistula (2) Urethra Valve Syndrome (6) Urethra, Diverticulum (1) Urogenital Sinus (2) Urorectal Septum Malformation Sequence (2) Urticaria Pigmentosa (9) Urticaria, Cold (1) Usher Syndrome Type II (1) * Uveitis (pars plantis -dots in vision) (3) * Uvulopalatopharyngoplasty (palate reconstruction) (2) VATER Syndrome or Vacterl Association (72) ** Vaccine Reaction to HIB Vaccine (6) * Vaccine Reaction to Measles Vaccine (9) * Vaccine Reaction to Pertussis (DPT) Vaccine (306) * Vaccine Reaction to Polio Vaccine (5) * Vaginal Cancer (2) * Vaginal Malformations (19) Vanishing Bile Duct Syndrome (1) Vanishing Twin Syndrome (5) Varicella-Zoster (Chickenpox), Fetal Effects (5)

76. GENATLAS GENE DATABASE RCN1, 11p13, reticulocalbin,Ca++ binding protein of the endoplasmic reticulum,involvedin protein processing,deleted in wagr syndrome, 602735, , -, y. http://bisance.citi2.fr/cgi-bin/mug?tex1=WT1

77. WAGR NETWORK LINK WELCOME TO THE REACHING OUT WAGR NETWORK LINK. THIS IS FOR ANY PERSONWISHING TO CONTACT OTHERS WITH KNOWLEDGE ABOUT wagr syndrome. http://groups.msn.com/WAGRNETWORKLINK

MSN Home My MSN Hotmail Search ... Money Groups WAGR NETWORK LINK WAGRNETWORKLINK@groups.msn.com Groups Home My Groups Language Help ... Tools SPONSORED SITES: Recommend This Group to a Friend WELCOME TO THE REACHING OUT WAGR NETWORK LINK. THIS IS FOR ANY PERSON WISHING TO CONTACT OTHERS WITH KNOWLEDGE ABOUT WAGR SYNDROME. THE DOCUMENTS HERE AT THIS LINK CONTAIN THE MEDICAL QUEST 2003 SURVERY CONDUCTED BY OUR NETWORK. THESE ARE MICROSOFT XL FILES AND CAN BE COPIED. WE ENCOURAGE IT. MICROSOFT VIEWER LINK: http://office.microsoft.com/downloads/2000/xlviewer.aspx OURWEBSITES WWW.WAGR.ORG http://members.aol.com/ReachingOutNet/ OUR E MAIL DISCUSSION GROUP IS http://groups.yahoo.com/group/WAGR FROM THERE YOU CAN FIND US! HOPE TO CONNECT WITH YOU SOON. SINCERELY, REACHING OUT, THE WAGR NETWORK New Messages View all Welcome Welcome to WAGR NETWORK LINK. Whether you are a manager, member, or visitor here, we hope you enjoy this MSN group. MSN Groups Tools Join This Group Recommend This Group Create Your Own Group ... Group Settings Notice: Microsoft has no responsibility for the content featured in this Group. Click here for more info.

78. Wagr, Syndrome : Arborescences MeSH Translate this page wagr, syndrome. Menu général CISMeF. néphroblastome C04.700.635 pageCISMeF du motclef wagr, syndrome C04.700.635.950 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/naviwagrsyndrome.html

Wagr, Syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF tumeurs syndromes néoplasiques héréditaires néphroblastome WAGR, syndrome ... WAGR, syndrome 27 février 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

79. Wagr-syndrome wagrsyndrome. From Date 15 Jan 2003 Time 111625 Remote Name 80.60.52.135.Comments. There was a question about wagr-syndrome in the 'old' discussionforum. http://www.chromosomehelpstation.com/_disc/00000003.htm

Chromosome Help-Station Discussion Home Contents Search Post ... Previous Up Wagr-syndrome From: Date: 15 Jan 2003 Time: Remote Name: Comments Last changed: January 26, 2003

80. Article Textbase No 10 Translate this page wagr (syndrome). TextBase ID 10, Auteur(s)ADICAP SNOMED Table des matières http://www.anapath.necker.fr/pathbase/french/textbase/BankArticles/HTML/10.html

WAGR (syndrome) TextBase ID: Auteur(s): ADICAP: SNOMED: Voir d'autres articles sur: Gene (s): Definition: L'acronyme WAGR ( References: TextBase

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