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         Beckwith-wiedemann Syndrome:     more detail
  1. Beckwith-Wiedemann syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Renee, MS Laux, 2005
  2. Section on Surgery. (Abstracts of Scientific Posters).(a discussion of a case of a patient with Beckwith-Wiedemann Syndrome): An article from: Southern Medical Journal
  3. Living with Beckwith-Wiedemann Syndrome (SuDoc HE 20.3152:B 38) by Nancy Weissman, 2001

21. HONselect - Beckwith-Wiedemann Syndrome
WiedemannBeckwith Syndrome - Beckwith Wiedemann Syndrome - Exomphalos MacroglossiaGigantism Syndrome - Syndrome, Beckwith-Wiedemann
http://www.hon.ch/HONselect/RareDiseases/C16.131.077.133.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Beckwith-Wiedemann Syndrome - Exomphalos-Macroglossia-Gigantism Syndrome
- Wiedemann-Beckwith Syndrome
- Beckwith Wiedemann Syndrome
- Exomphalos Macroglossia Gigantism Syndrome
- Syndrome, Beckwith-Wiedemann
- Syndrome, Exomphalos-Macroglossia-Gigantism
Français: Beckwith Wiedemann, syndrome Deutsch: Wiedemann-Beckwith-Syndrom - Exomphalos-Makroglossie-Gigantismus-Syndrom - EMG-Syndrom Español: Síndrome de Beckwith-Wiedemann - Síndrome de Exonfalo Macroglosia-Gigantismo Português: Síndrome de Beckwith-Wiedemann - Síndrome de Exonfalia-Macroglossia-Gigantismo HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: No Web sites: English Yes Français No Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C16.131.077.133.html Last modified: Wed May 18 2005

22. BBC NEWS Health Rare Disorder Risk For IVF Babies
According to New Scientist magazine, 37 were born with beckwithwiedemann syndrome (BWS). Four were IVF babies.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. Beckwith-Wiedemann Syndrome - Exomphalos-Macroglossia-Gigantism Syndrome - Infor
A syndrome of multiple defects characterized primarily by umbilical hernia ( A H
http://www.hon.ch/HONselect/RareDiseases/EN/C16.131.077.133.html
InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese
the word the part of word in MeSH term in MeSH term and description Information on "Beckwith-Wiedemann Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese
Beckwith-Wiedemann Syndrome Definition: A syndrome of multiple defects characterized primarily by umbilical hernia ( HERNA, UMBILICAL MACROGLOSSIA , and GIGANTISM and secondarily by visceromegaly, HYPOGLYCEMIA , and ear abnormalities.
Synonym(s): Exomphalos-Macroglossia-Gigantism Syndrome / Wiedemann-Beckwith Syndrome / Beckwith Wiedemann Syndrome / Exomphalos Macroglossia Gigantism Syndrome /
See also: Gigantism Hernia, Umbilical Macroglossia Genes, Wilms Tumor
See Related: Hernia, Umbilical Hypoglycemia Gigantism Macroglossia ... New search
Web resources for "Beckwith-Wiedemann Syndrome" English German = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - eMedicine - Beckwith-Wiedemann Syndrome : Article by Robert J Ferry, Jr, MD

24. Silencing Of CDKN1C (p57KIP2) Is Associated With Hypomethylation
R. Genesio, M. Bruggemann, W. Reik, and A. Riccio The twodomain hypothesis in beckwith-wiedemann syndrome autonomous imprinting of the
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

25. The Beckwith-Wiedemann Support Network Web Site
The BWSN is a nonprofit organization created for parents, professionals, andothers interested in the beckwith-wiedemann syndrome.
http://www.geocities.com/bwsn/
The BWSN is a non-profit organization created for parents, professionals, and others interested in the Beckwith-Wiedemann Syndrome.
For: - conference or clinic information -
- fundraising -
- help with insurance/legal issues -
please contact: Cheryl Hendrickson
Conferences and Fundraising Coordinator
Washington State, USA
email Cheryl Hendrickson
The Beckwith-Wiedemann Family Forum

26. Beckwith-Wiedemann Syndrome (www.whonamedit.com)
beckwithwiedemann syndrome A syndrome comprising gigantism, macroglossia andumbilical abnormalities in newborn, enlarged liver and spleen, hyperplasia of
http://www.whonamedit.com/synd.cfm/1198.html

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Beckwith-Wiedemann syndrome Also known as: Beckwith's syndrome Wiedemann’s syndrome Wiedemann-Beckwith syndrome Wiedemann-Beckwith-Combs syndrome Synonyms: Exomphalos-macroglossia-gigantism syndrome, familial macroglossia-omphalocele syndrome; macroglossia-omphalocele syndrome, macroglossia-omphalocele-visceromegaly syndrome. Associated persons: John Bruce Beckwith J. T. Combs Hans-Rudolf Wiedemann Description: Main symptoms are gigantism, macroglossia and umbilical abnormalities in newborn, enlarged liver and spleen, hyperplasia of the kidney, congenital abnormalities of the urinary tract, slight microcephaly, clonic seizures, often omphalocele (congenital hernia into the umbilical cord). Elements of congestive heart failure. Some patients develop hemihypertrophy, and there appears to be an increased risk of adrenal carcinoma, Wilm’s tumor, or other intra-abdominal neoplasms. Mental retardation may occur. Etiology unknown. Most cases sporadic, but autosomal dominant inheritance reported.

27. TheFetus.net - Beckwith-Wiedemann Syndrome -Sandra R Silva, MD & Philippe Jeanty
Comprehensive guide to prenatal ultrasound. Covers all aspects of sonography inpregnancy and the fetus.
http://www.thefetus.net/page.php?id=408

28. Beckwith-Wiedemann Syndrome
a CHORUS notecard document about beckwithwiedemann syndrome.
http://chorus.rad.mcw.edu/doc/00497.html
CHORUS Collaborative Hypertext of Radiology Multisystem entities About CHORUS
Search

Feedback
Beckwith-Wiedemann syndrome
  • big tongue
  • organomegaly (liver, kidneys, pancreas, heart)
  • omphalocele, umbilical hernia or diastasis recti
a/w Wilms tumor More info: Beckwith-Wiedemann syndrome [OMIM] Charles E. Kahn, Jr., MD - 24 November 1995
Last updated 26 May 2004
Related CHORUS documents:
Wilms tumor hemihypertrophy aniridia juvenile rheumatoid arthritis (JRA) ... nephroblastomatosis
Search for related articles:
AJR American Journal of Roentgenology PubMed : index to biomedical literature ...

Medical College of Wisconsin

29. Beckwith-Wiedemann Syndrome
beckwithwiedemann syndrome. big tongue; organomegaly (liver, kidneys, pancreas,heart) a/w Wilms tumor. More info beckwith-wiedemann syndrome OMIM
http://chorus.rad.mcw.edu/to-go/00497.html
Beckwith-Wiedemann syndrome
  • big tongue
  • organomegaly (liver, kidneys, pancreas, heart)
  • omphalocele, umbilical hernia or diastasis recti
a/w Wilms tumor More info: Beckwith-Wiedemann syndrome [OMIM] Home Multisystem entities

30. Beckwith-Wiedemann Syndrome
beckwithwiedemann syndrome is a consistent grouping of findings of unknown (cause)and characterized by a large tongue (), large organs () and large body
http://www.healthcentral.com/ency/408/001186.html
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Beckwith-Wiedemann syndrome
Definition: Beckwith-Wiedemann syndrome is a consistent grouping of findings of unknown etiology (cause) and characterized by a large tongue (

31. ► Beckwith-Wiedemann Syndrome
A medical encycopedia article on the topic beckwith-wiedemann syndrome.
http://www.umm.edu/ency/article/001186.htm
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Beckwith-Wiedemann syndrome
Overview Symptoms Treatment Prevention Definition:
Beckwith-Wiedemann syndrome is a consistent grouping of findings of unknown etiology (cause) and characterized by a large tongue ( macroglossia ), large organs ( visceromegaly ) and large body size ( macrosomia umbilical hernia or omphalocele (hernia of the navel), and low blood sugar in the newborn (neonatal hypoglycemia
Causes, incidence, and risk factors: The cause of Beckwith-Wiedemann syndrome is unknown, but it appears to be genetic. Some cases may be associated with a defect in chromosome number 11. Affected children are often large at birth. Many have an abdominal wall defect, such as an umbilical hernia or omphalocele. They have a characteristic facial appearance with a gaping mouth and large tongue. Infancy can be a critical period because of low blood sugar (hypoglycemia)

32. Beckwith-Wiedemann Syndrome
beckwithwiedemann syndrome (BWS) is an overgrowth disorder. The syndrome isusually sporadic, but may be inherited. The incidence of BWS has been reported
http://www.bws-support.org.uk/
Introduction
  • Beckwith-Wiedemann Syndrome (BWS) is an overgrowth disorder. The syndrome is usually sporadic, but may be inherited. The incidence of BWS has been reported as approximately 1:15,000 births The clinical picture of this syndrome can vary from mildly to greatly affected. The most common features are a large tongue, an abdominal wall defect and increased growth, but there are many others. These children are at risk for developing various types of tumours.
BWS Support Group - UK
This was started in 1990 by a group of parents with BWS children to share problems and information and to act as a self-help group. It aims to promote both public and professional awareness of BWS and to support and encourage research. The group has links with BWS groups in Holland and America. For further information about the group please contact: Bob and Gill Baker
Beckwith Wiedemann Support Group
The Drum and Monkey
Hazelbury Bryan
Dorset DT10 2EE Tel: 01258 817573 (evenings) 07889 211000 (mobile)
Fax: 01202 205325
E-mail: rbaker5165@aol.com

33. Beckwith-Wiedemann Syndrome
beckwithwiedemann syndrome. DESCRIPTION A syndrome of multiple defectscharacterized primarily by umbilical hernia, macroglossia, and gigantism and
http://www.5mcc.com/Assets/SUMMARY/TP0114.html
Beckwith-Wiedemann syndrome
DESCRIPTION: A syndrome of multiple defects characterized primarily by umbilical hernia, macroglossia, and gigantism and secondarily by visceromegaly, hypoglycemia, ear abnormalities, etc. Usual course - acute.
CAUSES:
  • unknown
Synonyms:
  • Beckwith syndrome
  • Wiedemann II syndrome
  • Exomphalos-macroglossia-gigantism syndrome
ICD-9-CM:
759.89 other specified anomalies
Author(s):
Mark R. Dambro, MD

34. Beckwith-Wiedemann Syndrome And Assisted Reproduction Technology (ART) -- Maher
Keywords beckwithwiedemann syndrome; ICSI; IVF; imprinting; methylation.beckwith-wiedemann syndrome (BWS) is a model imprinting disorder resulting from
http://jmg.bmjjournals.com/cgi/content/full/40/1/62

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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)
E R Maher L A Brueton S C Bowdin A Luharia W Cooper T R Cole F Macdonald J R Sampson C L Barratt W Reik and M M Hawkins Section of Medical and Molecular Genetics, University of Birmingham, Birmingham B15 2TT, UK
Institute of Medical Genetics for Wales, University of Wales College of Medicine, Cardiff CF14 4XN, UK
Reproductive Biology and Genetics Group, University of Birmingham, The Medical School, Birmingham B15 2TT, UK

35. J Med Genet -- Sign In Page
An imprinted gene p57KIP2 is mutated in beckwithwiedemann syndrome. Imprinting mutations in the beckwith-wiedemann syndrome suggested by altered
http://jmg.bmjjournals.com/cgi/content/full/42/8/648

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36. Beckwith-Wiedemann / Family Village / Library /
MEDLINEplus Medical Encyclopedia beckwithwiedemann syndrome Beckwith WiedemannSyndrome Beckwith-Wiedemann Family Forum Q A
http://www.familyvillage.wisc.edu/lib_beck.htm
Beckwith-Wiedemann Syndrome
Who to Contact
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Who to Contact
Beckwith-Wiedemann Support Network (BWSN)
2711 Colony Road
Ann Arbor, Michigan, USA 48104
(800) 837-2976 Parents Only
Fax: (734) 973-9721
Web: http://www.beckwith-wiedemann.org/
The Beckwith-Wiedemann Support Network provides information and peer support to people and families affected by Beckwith-Wiedemann Syndrome, works to increase public and professional awareness and encourages research into the cause, early (including prenatal) detection, and treatment of BWS. BWSN will assist persons who wish to start a support group in their locality and provides parent-to-parent matching by similar situations and /or geographic location. They also try to match families with older children who have BWS with new families, to provide support and encouragement. The Network publishes the Beckwith-Wiedemann Support Network newsletter three times a year, at no cost to members. Members also receive a family directory. BWSN also publishes a brochure, "What is Beckwith-Wiedemann Syndrome?"

37. Q & A About Beckwith-Wiedemann Syndrome, Cancer Facts 3.67
beckwithwiedemann syndrome (BWS) is a rare overgrowth syndrome that occurs inapproximately 1 in every 15000 births. A small number of infants and children
http://cis.nci.nih.gov/fact/3_67.htm
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Dictionary

Date reviewed: 8/28/2000
Questions and Answers About Living With Beckwith-Wiedemann Syndrome
  • What is Beckwith-Wiedemann Syndrome (BWS)? Beckwith-Wiedemann Syndrome (BWS) is a rare overgrowth syndrome that occurs in approximately 1 in every 15,000 births. A small number of infants and children with BWS develop cancer Most children have only a few of the many distinct characteristics of the syndrome. The most common characteristics, which can range from mild to severe, are:
    • Large tongue (macroglossia) Overall large body size with large organs Abdominal wall defects Above-average birth weight Uneven growth of limbs or organs (hemihypertrophy) Ear lobe creases or pits behind the upper ear Low blood sugar ( hypoglycemia ) shortly after birth Difficulty swallowing and eating Hearing loss Speech defects Occasional behavior abnormalities
    About 10 percent of children with BWS develop cancer (or 10 out of 100 children with BWS). Studies suggest that the period of highest risk for developing cancer is before the age of 4 years. The most common types of cancer that occur in children with BWS are Wilms’ tumor (kidney cancer) and hepatoblastoma liver cancer ). Other types of cancer, which occur more rarely, include adrenocortical
  • 38. Beckwith Wiedemann Syndrome
    beckwithwiedemann syndrome (BWS) is a rare genetic disorder. It may be characterizedby a wide spectrum of symptoms and findings that vary in range and
    http://www.bchealthguide.org/kbase/nord/nord52.htm
    var hwPrint=1;var hwDocHWID="nord52";var hwDocTitle="Beckwith Wiedemann Syndrome";var hwRank="1";var hwSectionHWID="nord52-Header";var hwSource="en-caQ2_05";var hwDocType="Nord";
    National Organization for Rare Disorders, Inc.
    Beckwith Wiedemann Syndrome
    Important
    It is possible that the main title of the report Beckwith Wiedemann Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
    Synonyms
    • Beckwith-Syndrome BWS EMG Syndrome Exomphalos-Macroglossia-Gigantism Syndrome Hypoglycemia with Macroglossia Macroglossia-Omphalocele-Visceromegaly Syndrome Omphalocele-Visceromegaly-Macroglossia Syndrome Visceromegaly-Umbilical Hernia-Macroglossia Syndrome Wiedmann-Beckwith Syndrome
    Disorder Subdivisions
    • None
    General Discussion
    Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder. It may be characterized by a wide spectrum of symptoms and findings that vary in range and severity from case to case. However, in many individuals with the syndrome, associated features may include above average weight and length at birth and/or increased growth after birth (postnatally); an unusually large tongue (macroglossia); enlargement of certain abdominal organs (visceromegaly); and/or abdominal wall defects. BWS may also be characterized by low blood sugar levels within the first days of life (neonatal hypoglycemia); advanced bone age, particularly up to age four; the presence of distinctive linear grooves in the ear lobes and/or other abnormalities of the facial area; and/or an increased risk of developing certain childhood cancers.

    39. Beckwith-Wiedemann Syndrome Definition - Medical Dictionary Definitions Of Popul
    Online Medical Dictionary and glossary with medical definitions.
    http://www.medterms.com/script/main/art.asp?articlekey=32868

    40. AllRefer Health - Beckwith-Wiedemann Syndrome
    beckwithwiedemann syndrome information center covers causes, prevention, symptoms,diagnosis, treatment, incidence, risk factors, signs, tests,
    http://health.allrefer.com/health/beckwith-wiedemann-syndrome-info.html

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    Definition Beckwith-Wiedemann syndrome is a consistent grouping of findings of unknown etiology (cause) and characterized by a large tongue ( macroglossia ), large organs ( visceromegaly ) and large body size ( macrosomia umbilical hernia or omphalocele (hernia of the navel), and low blood sugar in the newborn (neonatal hypoglycemia
    Beckwith-Wiedemann Syndrome
    Metopic Ridge The cause of Beckwith-Wiedemann syndrome is unknown, but it appears to be genetic. Some cases may be associated with a defect in

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