81. Cancer Syndromes wagr syndrome ANIRIDIA AND ABSENT PATELLA deletion of 11p13 resultsin the wagr syndrome Aniridia; AN1 by OMIM Shaw et al. http://ibis-birthdefects.org/start/cancersy.htm

Tips for printing Cancer Syndromes About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and Nephroblastoma Aniridia,Type II Wims Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Wilms Tumor 3 Wilms Tumor 2 Multiple Tumor Associated Chromosome Region 1 Special Resources Cancer Syndrome A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Groups Online Mendelian Inheritance in Man by OMIM ANIRIDIA ... ANIRIDIA, CEREBELLAR ATAXIA ... WAGR SYNDROME ... ANIRIDIA AND ABSENT PATELLA ... WILMS TUMOR 1 ... ECTOPIA PUPILLAE ... CAT EYE SYNDROME ... PETERS ANOMALY ... EXOSTOSES ... SPLIT-HAND/FOOT ... Wilms Tumor Nephroblastoma by OMIM Rather numerous instances of multiple sibs with Wilms tumor have been described ... The syndrome of aniridia, hemihypertrophy and other congenital anomalies with Wilms tumor, subsequently known as the WAGR syndrome, was first described by Miller et al. (1964) ... . Riccardi et al. (1978) observed a triad of aniridia, ambiguous genitalia and mental retardation (AGR triad) in 3 patients with an interstitial deletion of the short arm of chromosome 11 ... Marshall et al. (1982) studied 14 patients with aniridia .... 6 had interstitial deletion of 11p of various lengths. Band 11p13 was included in the deletion in all 6 cases ...

82. JCO -- Abstracts: Breslow Et Al. 21 (24): 4579 We compared demographics, disease characteristics, and treatment outcomes ina large cohort of WT patients who did or did not have the wagr syndrome. http://www.jco.org/cgi/content/abstract/21/24/4579

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 Subscribe ... Email this article to a colleague Similar articles found in: JCO Online PubMed PubMed Citation Search Medline for articles by: Breslow, N. E. Nichols, K. E. Alert me when: new articles cite this article Download to Citation Manager Journal of Clinical Oncology , Vol 21, Issue 24 (December), 2003: 4579-4585 American Society for Clinical Oncology Characteristics and Outcomes of Children With the Wilms Tumor-Aniridia Syndrome: A Report From the National Wilms Tumor Study Group Norman E. Breslow Robin Norris Patricia A. Norkool Tammy Kang J. Bruce Beckwith Elizabeth J. Perlman Michael L. Ritchey Daniel M. Green Kim E. Nichols Address reprint requests to Norman Breslow, PhD, Department of Biostatistics, Box 357232, University of Washington, Seattle, WA 98195-7232; e-mail: norm@u.washington.edu

83. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=WAGR+Syndrome More results from www.nlm.nih.gov MeSHD terms associated to MeSH-C term wagr syndromeMeSH-D terms associated to MeSH-C term wagr syndrome, G2D Home. The number indicatesthe strength of the association of the corresponding term to wagr syndrome. http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=WAGR Syndrome

84. Pediatric Research -- Abstracts: Kohler Et Al. 45 (2): 187 Mutations in the WT1 gene causing Wilms tumors were first reported in wagr syndrome(Wilms tumor, Aniridia, Genitourinary malformation, mental Retardation) and http://www.pedresearch.org/cgi/content/abstract/45/2/187

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Submit correspondence regarding this article Similar articles found in: Pediatric Research Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Kohler, B. Gruters, A. Alert me when: new articles cite this article Download to Citation Manager ARTICLES Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene B Kohler, V Schumacher, U Schulte-Overberg, W Biewald, T Lennert, D l'Allemand, B Royer-Pokora and A Gruters Department of Pediatric Endocrinology, Humboldt Universitat zu Berlin, Germany. Mutations in the WT1 gene causing Wilms tumors were first reported in WAGR syndrome (Wilms tumor, Aniridia, Genitourinary malformation, mental Retardation) and Denys Drash syndrome (pseudohermaphroditism, Wilms tumor, nephropathy), but only in a few patients with hypospadias and cryptorchidism without other signs of Denys Drash (DDS) or WAGR syndrome WT1 mutations were identified. We report a boy, who was born in 1989 with

85. WAGR, Syndrome : Arborescences MeSH Translate this page wagr, syndrome arborescences MeSH. Menu général CISMeF. wagr, syndromeC11.941.375.060.950 page PubMed du motclef page CISMeF du motclef http://www.chu-rouen.fr/navimesh/W/naviwagrsyndrome.html

WAGR, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF tumeurs tumeurs par types histologiques tumeur complexe et mixte néphroblastome ... WAGR, syndrome 07 janvier 2004 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

86. Aniridia Network International - Aniridic Keratopathy wagr. every 3 months until they are 6 years of age.6 Children with Wilms AniridiaGenitourinaryabnormalities-(mental) Retardation (wagr) syndrome are at http://www.aniridia.org/conditions/wagr.html

Supporting people with aniridia and their Families Just Diagnosed? click here Homepage About Us About Aniridia ... The Aniridia Directory Contact Details Aniridia Network PO Box 6444 Colchester UK Tel: (+44) 07779 859 624 hannah@aniridia.org WAGR W ilms' tumour, A niridia, G enitourinary abnormalities/Gonadoblastoma and R etardation Also know as Wilms' Tumour - Aniridia - Genitourinary Anomalies-MR Syndrome. Chromosome 11p deletion syndrome AGR syndrome Wilms' Tumour Aniridia syndrome Miller Syndrome What is WAGR? WAGR is a very rare genetic condition. The letters represent the first letters of each of the four main symptoms Wilm tumour This is a malignant cancer of the kidneys and is the most common renal tumor in both children that is rarely diagnosed after the age of 12. It is also one of the most treatable cancers especially if it is caught at an early stage. It is caused by the deletion of the wilms tumour suppressor gene WT1. This gene appears to play an important role in the normal development and maturation of the kidneys and gonads (See below). According to the National Cancer Institute (USA) "Patients with aniridia or hemihypertrophy should be screened with ultrasound every 3 months until they are 6 years of age.[6] Children with Wilms' Aniridia-Genitourinary abnormalities-(mental) Retardation (WAGR) syndrome are at increased risk of eventually developing renal failure and should be monitored. Patients with Wilms' tumor and aniridia without genitourinary abnormalities are at lesser risk but should be monitored." (natioanl Cancer Institute -

87. WAGR-oireyhtymä WILMS TUMOR ANIRIDIA - GENITOURINARY ANOMALIES - MENTAL RETARDATION syndrome Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation syndrome wagr Complex. http://www.saunalahti.fi/kup/syndroma/wagr.htm

Kehitysvammahuollon tietopankki WAGR-oireyhtymä WILMS TUMOR - ANIRIDIA - GENITOURINARY ANOMALIES - MENTAL RETARDATION SYNDROME Wilms' Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome WAGR Complex WAGR-oireyhtymä on harvinainen sairaus, jonka nimi tulee englanninkielisistä sanoista W ilms tumor ( Wilmsin kasvain A niridia ( silmän värikalvon puuttuminen ), G enitourinary abnormalities ( epämuodostuneet suku- ja virtsaelimet ) ja Mental R etardation ( kehitysvammaisuus ). Nimi antaa hyvän kuvan sairauden ilmenemistavasta. Oireet voivat tosin jossain määrin vaihdella ja niitä voi olla enemmänkin. WAGR-oireyhtymä johtuu useimmiten sattumanvaraisesta sikiökehityksen aikaisesta mutaatiosta. Joissakin hyvin harvinaisissa tapauksissa on tavattu autosomaalisesti vallitsevaa periytyvyyttä Tämä v. 1964 ensimmäisen kerran kuvattu oireyhtymä on useamman geenin vaurion aiheuttama. Lisätietoja: WAGR Syndrome, OMIM WAGR Syndrome, NORD Fetaalinen aivoproteiini 239, Kehitysvammahuollon tietopankki Kari Viitapohja 9.1.1998, 19.6.2000, 8.12.2002 Kehitysvammaisten Uudenmaan tukipiiri ry.

88. Chromosome 11p Deletion Syndrome Wilms tumoraniridia-genitourinary abnormalities-mental retardation triad. Wilmstumor-aniridia-gonadoblastoma-mental retardation (wagr) syndrome, association. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome160.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome chromosome 11p deletion syndrome Synonyms 11p- syndrome 11p deletion syndrome chromosome 11p monosomy del(11p) syndrome deletion 11p syndrome monosomy 11p partial monosomy 11p aniridia type II aniridia-ambiguous genitalia-mental retardation (AGR) syndrome, triad aniridia-genitourinary-abnormalities-mental retardation triad aniridia-Wilms tumor association, syndrome (aniridia-WT association, AWTA) aniridia-Wilms tumor-gonadoblastoma syndrome del11/aniridia complex oculocerebrorenal (OCR) syndrome Brusa-Toricelli syndrome Miller syndrome Wilms tumor-aniridia syndrome Wilms tumor-aniridia-genitourinary abnormalities-mental retardation triad Wilms tumor-aniridia-gonadoblastoma-mental retardation (WAGR) syndrome, association Summary Deletion of the short arm of chromosome 11 with a variable phenotype: Congenital absence of the iris, genitourinary abnormalities and mental retardation known as aniridia-ambiguous genitalia-mental retardation (AGR) triad; Wilms tumor-aniridia-ambiguous genitalia-mental retardation (WAGR) syndrome; Wilms tumor associated with congenital absence of the iris, genitourinary abnormalities, hemihypertrophy, mental retardation, and other anomalies termed AWTA; Major Features Head and neck: Cranial asymmetry, microcephaly, brachycephaly, prominent forehead, long narrow face, large fontanelles, premature synostosis of metopic sutures, and biparietal foramina.

89. NORD - National Organization For Rare Disorders, Inc. Search NORD s Databases Read about diseases in NORD s Rare DiseaseDatabase. Find an organization in our Organizational Database. http://www.rarediseases.org/search/zcat_search_results?allfields=medulloblastoma

90. Gimenei >> Health >> Conditions_and_Diseases >> Neurological_Disorders >> Chromo Gimenei.com, Search for Scope All Words, Results per page 10.Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Neurological

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Neurological Disorders ... Chromosomal WAGR Syndrome Music: The Hyperion Schubert Edition 13 / Marie McLaughlin, Graham Johnson - This is a fine opera. It is also well performed, and for an old recording, the sound quality is pretty good. It's also dirt cheap. Video Games: The Legend of Zelda: The Wind Waker

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 5     81-90 of 90    Back | 1  | 2  | 3  | 4  | 5