Www.ohsu.edu/cliniweb/C11/C11.250.60.html www.dictionarybarn.com/WAGRSYNDROME.php SearchBug Directory Health Conditions_and_Diseases Search wagr syndrome, wagr syndrome - http//www.wagr.org Information forfamilies or physicians interested in learning more about wagr syndrome. http://www.ohsu.edu/cliniweb/C11/C11.250.60.html
Health Library - wagr syndrome. 3 affiliated groups. Founded 2000. Provides information andsupport to persons with wagr syndrome or aniridia, and their families. http://healthlink.uhseast.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29w
Results Of The Search wagr syndrome, Wilms tumor, aniridia, gonadoblastoma, mental retardation a reviewapropos of 2 cases MC Mochon T Philip Pediatrie 1987 ;42(4);24952. http://invention.swmed.edu/trite/abstracts/user-1015659130/results.shtml
Health Library - wagr syndrome. Important It is possible that the main title of thereport wagr syndrome is not the name you expected. Please check http://myhealth.barnesjewish.org/library/healthguide/illnessconditions/topic.asp
Health Library - wagr syndrome. 3 affiliated groups. Founded 2000. Provides information andsupport to persons with wagr syndrome or aniridia, and their families. http://myhealth.barnesjewish.org/library/healthguide/selfhelp/topic.asp?hwid=shc
Mental Retardation, Directory wagr syndrome. wagr syndrome, OMIM wagr syndrome, NORD Waisman Syndrome. PARKINSONISM,EARLYONSET, WITH MENTAL RETARDATION, OMIM, Victor A. McKusick. http://www.saunalahti.fi/kup/engl/webs_w.html
Wilms' Tumour - Genetics Wilms tumor and wagr syndrome. Medline Search wagr syndrome (PubMed) Limit searchto Last Year Limit search to Last 2 Years Limit search to Reviews http://www.cancerindex.org/geneweb/X210202.htm
Extractions: Familial Wilms' tumour (defined as either bilateral disease or a family history of Wilms' tumour) account for approximately 5% of cases. For those with sporadic (unilateral) disease the risk of Wilms' tumour among their offspring is low: in a series of 179 children from 96 survivors of unilateral Wilms' (Li, 1988) non had developed the disease (upper 95% CI 2%). Children with
NodeWorks - Neurological Disorders: Chromosomal: WAGR Syndrome mental retardation (R). 1. NORD wagr syndrome Offers the synonyms,a general discussion and further resources. thumbnail, 2. Reaching http://dir.nodeworks.com/Health/Conditions_and_Diseases/Neurological_Disorders/C
Extractions: in entire NodeWorks Directory in Health in Neurological Disorders in Chromosomal in ++ WAGR Syndrome Top Health Neurological Disorders Chromosomal WAGR Syndrome A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), ANIRIDIA (A), genitourinary abnormalities (G), and mental retardation (R). NORD: WAGR Syndrome Offers the synonyms, a general discussion and further resources. Reaching Out - The WAGR Network Parent support network for families and professionals looking for information about WAGR Syndrome/Aniridia. WAGR Syndrome Information for families or physicians interested in learning more about WAGR Syndrome. Yahoo! Groups : WAGR Syndrome A brief description of this support group. Join, post and read messages.
New Page 1 wagr syndrome assoicated to Health Just The Best Results from the LinkspiderOrganization. Click here for wagr syndrome assoicated to Health Websites. http://www.linkspider.org/index.cgi/Health/ConditionsandDiseases/NeurologicalDis
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Principal's Office: Welcome (University Of Dundee) gene, WT1, was first identified in 1990 because of its involvement in chromosomaldeletions in children suffering from the wagr syndrome (Wilms tumour, aniridia http://www.dundee.ac.uk/principalsoffice/discoverydays/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
Descripteur : WAGR Syndrome = WAGR, SYNDROME Descripteur wagr syndrome = WAGR, SYNDROME Définition NLM A contiguous genesyndrome associated with hemizygous deletions of chromosome region 11p13. http://www.saphirdoc.ch/Thesaurus.htm&numrec=051188968936070
A To Z Encyclopedia Topic: Wilms` Tumor wagr syndrome the acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Wilms` Tumor
Wilms Tumor - Lucile Packard Children's Hospital wagr syndrome The acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored part http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/oncology/wilms.html
Extractions: What is Wilms tumor? Wilms 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 Wilms 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 Wilms 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 Wilms tumor, both kidneys are involved. What causes Wilms tumor?
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Oncology wagr syndrome the acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored part http://www.rush.edu/rumc/page-P02747.html
Extractions: Wilms Tumor Wilms 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 500 children in the US are diagnosed with Wilms 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 Wilms 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 Wilms tumor, both kidneys are involved. It is uncommon for Wilms tumor to run in families. Less than 2 percent of cases will have an affected relative. Most cases of Wilms tumor are considered sporadic (occur by chance) and are the result of genetic mutations that affect cell growth in the kidney. These mutations generally arise after birth, but, in some cases, children are born with a genetic alteration that predisposes them to cancer. A small percentage of patients with Wilms tumor have one of three genetic syndromes, including the following:
Aniridia a fourth type associated with Wilms tumor, genital abnormalities, and deletionof 11p13 ( wagr syndrome ) term WAGR WAGR is a syndrome .. http://ibis-birthdefects.org/start/aniridia.htm
Extractions: Shaw et al. (1960) ascertained 176 cases of aniridia in the lower Michigan peninsula ... mutation rate about 4 x 10(-6) per gamete per generation. Affected persons may be visually handicapped because of nystagmus, cataract or glaucoma ... Undoubtedly more than one "cause" of aniridia exists ... Gove et al. (1961) identified 77 cases of aniridia descended from an affected woman born in 1824 ... Delleman and Winkelman (1973) emphasized that atypical colobomata and slitlike defects of the iris stroma may be partial expressions of aniridia ... a fourth type associated with Wilms tumor, genital abnormalities, and deletion of 11p13 ( WAGR syndrome ) ...
