61. Beckwith-Wiedemann Syndrome Beckwith Wiedemann syndrome (BWS) is a fetal overgrowth disorder Renal abnormalitiesin beckwithwiedemann syndrome are associated with 11p15.5 http://www.humpath.com/article.php3?id_article=824

62. American Journal Of Speech-Language Pathology: Articulation In Beckwith-Wiedeman Full text of the article, Articulation in beckwithwiedemann syndrome Two casestudies from American Journal of Speech-Language Pathology, a publication http://www.findarticles.com/p/articles/mi_qa3856/is_200008/ai_n8920464

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles American Journal of Speech-Language Pathology Aug 2000 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports Articulation in Beckwith-Wiedemann syndrome: Two case studies American Journal of Speech-Language Pathology Aug 2000 by Van Borsel, John Morlion, Bieke Van Snick, Kathleen Leroy, Jules S Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. Beckwith-Wiedemann syndrome (BWS) is a genetic disorder with abdominal wall defects, gigantism, and macroglossia as its main characteristics. A number of investigators have reported the presence of articulation errors in individuals with BWS due to macroglossia. However, few data are available on the exact nature of the articulation problems of subjects with BWS. This paper presents two case studies that highlight the articulatory characteristics associated with BWS. Subjects were a boy aged 5 years 9 months and a girl aged 3 years 6 months. A phonetic analysis was conducted in which it was found that primarily consonants with an anterior place of articulation were affected. The error patterns appeared to be related to inappropriate tongue and lip postures. An observer experiment in which naive and expert observers rated speech samples from three modes of presentation (auditory-only, visual-only, and audiovisual) showed that the subjects' speech was more disturbed visually than auditorily.

63. Entrez PubMed beckwithwiedemann syndrome (BWS) is a congenital cancer-predisposition syndrome Abdomen/abnormalities; beckwith-wiedemann syndrome/complications* http://www.reproductive-health-journal.com/pubmed/11813134

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64. Entrez PubMed beckwithwiedemann syndrome/etiology*; Case-Control Studies; Female; Fertilizationin Vitro/adverse effects*; Genomic Imprinting*; Humans; Male; Pregnancy http://www.reproductive-health-journal.com/pubmed/15284956

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65. Ascertainment Of The Incidence Of Beckwith-Wiedemann Syndrome In The National Wi Patients were classified as having beckwithwiedemann syndrome (BWS) if they werereported as such by their primary treating oncologist. http://www.jco.org/cgi/content/full/19/2/593-a

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 (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 Grundy, R. Articles by Diller, L. Journal of Clinical Oncology , Vol 19, Issue 2 (January), 2001: 593-594 American Society for Clinical Oncology SPECIAL DEPARTMENTS Ascertainment of the Incidence of Beckwith-Wiedemann Syndrome in the National Wilms Tumor Study Group Richard Grundy Jon Pritchard Institute of Child HealthUniversity of BirminghamBirmingham, United Kingdom Institute of Child HealthLondon, United Kingdom To the Editor: In the study by Porteus et al published in the May 2000 issue of the Journal of Clinical Oncology the authors assume a correct diagnosis of Beckwith-Wiedemann syndrome (BWS) from National Wilms Tumor Study Group (NWSTG) data sheets completed by registering physicians at the time of diagnosis. Apparently, there was no

66. Characteristics And Outcome Of Children With Beckwith-Wiedemann Syndrome And Wil PURPOSE Children with beckwithwiedemann syndrome (BWS) are at increased Ascertainment of the Incidence of beckwith-wiedemann syndrome in the National http://www.jco.org/cgi/content/abstract/18/10/2026

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 ... Cited by other online articles PubMed PubMed Citation Articles by Porteus, M. H. Articles by Diller, L. Journal of Clinical Oncology , Vol 18, Issue 10 (May), 2000: 2026-2031 American Society for Clinical Oncology By Matthew H. Porteus Patricia Narkool Donna Neuberg Katherine Guthrie Norman Breslow Daniel M. Green Lisa Diller Address reprint requests to Lisa Diller, MD, Dana-Farber Cancer Institute, 44 Binney St, Boston, MA 02115; email Lisa_Diller@ dfci.harvard.edu. PURPOSE: Children with Beckwith-Wiedemann syndrome (BWS) are reviewed the National Wilms Tumor Study Group (NWTSG) records to assess clinical characteristics and outcome of patients with WT and BWS.

67. IVF Raises Risk Of Beckwith Wiedemann Syndrome Children conceived by IVF are nine times as likely to have the very rare disorderbeckwithwiedemann syndrome as those conceived naturally, according to a http://www.medicalnewstoday.com/medicalnews.php?newsid=12067

68. Beckwith-wiedemann Syndrome - Definition From Biology-Online.org Definition and other additional information on beckwithwiedemann syndrome fromBiology-Online.org dictionary. http://www.biology-online.org/dictionary/beckwith-wiedemann_syndrome

Forum Tutorials Dictionary Directory ... B beckwith-wiedemann syndrome Beckwith-Wiedemann syndrome (Science: syndrome) This syndrome , of unknown cause , is characterised by a group of the following findings large tongue ... visceromegaly ), large body size umbilical hernia and neonatal hypoglycaemia . Evidence suggests a genetic lesion Birth weight is often more than 8 pounds Complications include Wilm's tumour seizures aspiration and hypoglycaemia. Search the dictionary About Us Contact Us Link to Us Chemistry ... Equations

69. Indian Pediatrics - Editorial Incomplete beckwithwiedemann syndrome in a Child with Orbital Rhabdomyosarcoma beckwith-wiedemann syndrome (BWS) was first recognized as a syndrome by http://www.indianpediatrics.net/mar2002/mar-299-304.htm

Home Past Issue About IP About IAP ... Subscription Case Reports Indian Pediatrics 2002; 39:299-304 Incomplete Beckwith-Wiedemann Syndrome in a Child with Orbital Rhabdomyosarcoma V. Thavaraj Anitha Sethi* L.S. Arya From the Division of Pediatric Oncology, Department of Pediatrics and *Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110 029, India. Correspondence to: Dr. V. Thavaraj, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110 029, India. E-mail: sowmyam@mantraonline.com Manuscript received: May 31, 2001; Initial review completed: July 18, 2001; Revision accepted: September 5, 2001. Beckwith-Wiedemann syndrome (BWS) was first recognized as a syndrome by Beckwith in 1963, when he reported autopsy findings on three unrelated children with omphalocele, macroglossia, cytomegaly of adrenal cortex, renal medullary hyperplasia and hyperplastic visceromegaly(1). In 1964 Wiedemann published an article on the same syndrome in three siblings with omphalocele, macrosmia and neonatal hypoglycemia(2). The incidence of BWS has been estimated to be 1:13700 live births(3). The increased risk of tumor formation in BWS patients is estimated to be 7.5%(4) and the risk is further increased to 10% if hemihypertrophy is present(4). It has been suggested that BWS can be inherited by the homozygous state of an autosomal recessive mutation(5). We describe a rare case report of partial expression of BWS associated with orbital rhabdomyosarcoma (RMS).

70. Human KVLQT1 Gene Shows Tissue-specific Imprinting And Encompasses Beckwith-Wied Allelic methylation of H19and IGF2in the beckwithwiedemann syndrome. Imprinting mutations in the beckwith-wiedemann syndrome suggested by an altered http://www.nature.com/ng/journal/v15/n2/abs/ng0297-181.html

@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 Letter Nature Genetics doi:10.1038/ng0297-181 Human gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements Maxwell P. Lee , Ren-JuHu Hu , Laura A. Johnson Genomic imprinting is an epigenetic chromosomal modification in the gamete or zygote causing preferential expression of a specific parental allele in somatic cells of the offspring. We and others have identified three imprinted human genes on 11p15.5, (refs 1-4), (refs 1,5), and (ref. 6), although the latter gene is separated by 700 kb from the other two, and it is unclear whether there are other imprinted genes within this large interval. We previously mapped an embryonal tumour suppressor gene to this region7, as well as five balanced germline chromosomal rearrangement breakpoints from patients with Beckwith-Wiedemann syndrome (BWS)8, a condition characterized by prenatal overgrowth and cancer. We isolated the upstream exons of the previously identified gene , which causes the familial cardiac defect long-QT (LQT) syndrome. We found that

71. Beckwith-Wiedemann Syndrome beckwithwiedemann syndrome. BWS. EMG syndrome beckwith-wiedemann syndrome A 23 week fetus with Beckwith-Weidemann syndrome and associated severe http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=40

72. Entrez PubMed beckwithwiedemann syndrome/etiology*; beckwith-wiedemann syndrome/genetics;Cohort Studies; Comparative Study; Female; Fertilization in Vitro/adverse http://www.jexpclinassistreprod.com/pubmed/12525545

My NCBI [Sign In] [Register] All Databases ... Books Search PubMed Protein Nucleotide Structure Genome Books CancerChromosomes Conserved Domains 3D Domains Gene Genome Project GENSAT GEO Profiles GEO DataSets HomoloGene Journals MeSH NCBI Web Site NLM Catalog OMIA OMIM PMC PopSet Probe PubChem BioAssay PubChem Compound PubChem Substance SNP Taxonomy UniGene UniSTS for Limits Preview/Index History Clipboard Details About Entrez Text Version Entrez PubMed Overview FAQ Tutorial New/Noteworthy ... E-Utilities PubMed Services Journals Database MeSH Database Single Citation Matcher Batch Citation Matcher ... Cubby Related Resources Order Documents NLM Mobile NLM Catalog NLM Gateway ... PubMed Central Display Summary Brief Abstract Citation MEDLINE XML UI List LinkOut ASN.1 Related Articles Cited Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Gene (GeneRIF) Links Genome Links Project Links GENSAT Links GEO Profile Links HomoloGene Links Nucleotide Links OMIA Links OMIM Links BioAssay Links Compound Links Compound via MeSH Substance Links Substance via MeSH PMC Links Cited in PMC PopSet Links Probe Links Protein Links SNP Links Structure Links UniGene Links UniSTS Links Show Sort by Author Journal Pub Date Send to Text File Clipboard E-mail Order All: 1 Review: J Med Genet.

73. Molecular Genetics And Epigenetics Of Beckwith-Wiedemann Syndrome Molecular genetics and epigenetics of beckwithwiedemann syndrome. Dr. MichaelHiggins Department of Cancer Genetics, Roswell Park Cancer Institute http://www.uofa-medical-genetics.org/news/article.php?article=115

74. Arch Pediatr Adolesc Med -- Abstract: Beckwith-Wiedemann Syndrome In A Mother An The beckwithwiedemann syndromeexomphalos, macroglossia and gigantismoccurredin a mother and her son. The clinical and metabolic features of this http://archpedi.ama-assn.org/cgi/content/abstract/131/7/801

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 131 No. 7, July 1977 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager Articles in PubMed by Ben-Galim E Abrahamov A Contact me when this article is cited Beckwith-Wiedemann syndrome in a mother and her son E. Ben-Galim, E. Gross-Kieselstein and A. Abrahamov The Beckwith-Wiedemann syndromeexomphalos, macroglossia and gigantismoccurred in a mother and her son. The clinical and metabolic features of this syndrome are described. We believe this is the first report of this syndrome affecting a mother and her son. An autosomal dominant pattern of inheritance is suggested. HOME CURRENT ISSUE PAST ISSUES COLLECTIONS ... HELP

75. Intrauterine Growth And Ultrasound Findings In Fetuses With Beckwith-Wiedemann S RESULTS Nine infants with beckwithwiedemann syndrome had antenatal ultrasound Two infants were suspected to have beckwith-wiedemann syndrome in utero. http://www.greenjournal.org/cgi/content/abstract/89/4/538

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76. Beckwith-Wiedemann Syndrome, Placental Abnormalities, And Gestational Proteinuri BACKGROUND beckwithwiedemann syndrome is a genetically complex congenital All three infants had features diagnostic of beckwith-wiedemann syndrome. http://www.greenjournal.org/cgi/content/abstract/83/5/813

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77. Sao Paulo Medical Journal - beckwithwiedemann syndrome is a congenital disorder first recognized in 1964 by Monitoring the glycemia in beckwith-wiedemann syndrome newborns every 6 http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802003000300010

78. Beckwith Wiedemann Syndrome beckwithwiedemann syndrome. In Buyse ML, ed. Beckwith-Wiedemannsyndrome EMG (exomphalos-macroglossia-gigantism) syndrome. In Syndromes of the Head http://ibis-birthdefects.org/start/ukrainian/ubeckwit.htm

Please set browser to encoding in cyrillic) [EMG (åêçîìôàëîñ-ìàêðîãëîñ³ÿ-ã³ãàíòèçì) ñèíäðîì; ³äåìàíà-Áåêâ³òà ñèíäðîì] "В новинах" ÁÂÑ - ïðèêëàä ³ìïðèíòèíãó ó ëþäèíè. ³í ìîæå áóòè ñïðè÷èíåíèé dup 11p15 áàòüê³âñüêîãî ïîõîäæåííÿ, áàòüê³âñüêîþ (óí³ïàðåíòàëüíîþ) äèñî쳺þ ðåã³îíó 11ð15.5 àáî çìåíøåíèì ³ìïðèíòóâàííÿì ìàòåðèíñüêîãî àëåëÿ (ãåíè, ùî ìîæóòü â³ä³ãðàâàòè ðîëü - IGF-2, H-19, KVLQT-1, P 57k1p2). Îñê³ëüêè äóïë³êîâàíèé ðåã³îí ì³ñòèòü ëîêóñ ³íñóë³íó, ³íñóë³íîïîä³áíîãî ðîñòîâîãî ôàêòîðà-2 (IGF-2), öå íàøòîâõóº íà äóìêó, ùî îñíîâí³ ïðîÿâè ÁÂÑ ìîæóòü áóòè ñïðè÷èíåí³ íàäëèøêîì îäíîãî àáî îáîõ. Êð³ì òîãî, áóëî âñòàíîâëåíî, ùî ãåí ³íñóë³íó ³ ñ-Íà-ras-1 îíêîãåí òàêîæ çíàõîäÿòüñÿ íà êîðîòêîìó ïëå÷³ õðîìîñîìè 11. Íåçáàëàíñîâàíà ê³ëüê³ñòü ìàòåðèíñüêèõ ³ áàòüê³âñüêèõ àëåëåé ìîæå áóòè çàãàëüíèì ôàêòîðîì â ð³çíèõ åò³îëîã³÷íèõ ôîðìàõ ÁÂÑ ³ àñîö³éîâàíèõ ç íèì ïóõëèíàõ. Best LG. Familial posterior helical ear pits and Wiedeman-Beckwith syndrome. American Journal of Medical Genetics 1991;40:188-195. Butler MG. Beckwith-Wiedemann Syndrome. In: Buyse ML, ed. Birth Defects Encyclopedia. Dover: Center for Birth Defects Information Services, Inc., 1990:218-219.

79. BrainTalk Communities - Beckwith-Wiedemann Syndrome Online patient support groups for healthcare and neurology. http://brain.hastypastry.net/forums/archive/index.php/t-167.html

BrainTalk Communities Specific Neurological Conditions (M - Z) Overgrowth Syndrome PDA View Full Version : Beckwith-Wiedemann Syndrome ~Pansy~ 03-11-2004, 10:42 PM Beckwith-Wiedemann Support Network (http://www.beckwith-wiedemann.org/index.html)

80. Short Description Of Cell Lines. Pathology: Beckwith-Wiedemann Syndrome #130650 Pathology beckwithwiedemann syndrome 130650 OMIM record. - By selecting thecell line name, you will receive the detailed description of the cell line http://www.biotech.ist.unige.it/cldb/pat218.html

Version Short description of cell lines. Pathology: Beckwith-Wiedemann syndrome OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser IMG-1215 human skin, fibroblast MWCMG ... By Beatrice...

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