 Beckwith-Wiedemann Syndrome
"Beckwith-Wiedemann Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.
| Descriptor ID |
D001506
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| MeSH Number(s) |
C16.131.077.133 C16.131.260.080 C16.320.180.080
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| Concept/Terms |
Beckwith-Wiedemann Syndrome- Beckwith-Wiedemann Syndrome
- Beckwith Wiedemann Syndrome
- Syndrome, Beckwith-Wiedemann
- Wiedemann-Beckwith Syndrome
- Syndrome, Wiedemann-Beckwith
- Wiedemann Beckwith Syndrome
- Wiedemann-Beckwith Syndrome (WBS)
- Syndrome, Wiedemann-Beckwith (WBS)
- Syndromes, Wiedemann-Beckwith (WBS)
- Wiedemann Beckwith Syndrome (WBS)
- Wiedemann-Beckwith Syndromes (WBS)
- Exomphalos-Macroglossia-Gigantism Syndrome
- Exomphalos Macroglossia Gigantism Syndrome
- Exomphalos-Macroglossia-Gigantism Syndromes
- Syndrome, Exomphalos-Macroglossia-Gigantism
- Syndromes, Exomphalos-Macroglossia-Gigantism
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Below are MeSH descriptors whose meaning is more general than "Beckwith-Wiedemann Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Beckwith-Wiedemann Syndrome".
This graph shows the total number of publications written about "Beckwith-Wiedemann Syndrome" by people in this website by year, and whether "Beckwith-Wiedemann Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1992 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2012 | 0 | 1 | 1 |
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Below are the most recent publications written about "Beckwith-Wiedemann Syndrome" by people in Profiles.
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Arboleda VA, Lee H, Parnaik R, Fleming A, Banerjee A, Ferraz-de-Souza B, Délot EC, Rodriguez-Fernandez IA, Braslavsky D, Bergadá I, Dell'Angelica EC, Nelson SF, Martinez-Agosto JA, Achermann JC, Vilain E. Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome. Nat Genet. 2012 May 27; 44(7):788-92.
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Manjila S, Chim H, Eisele S, Chowdhry SA, Gosain AK, Cohen AR. History of the Kleeblattschädel deformity: origin of concepts and evolution of management in the past 50 years. Neurosurg Focus. 2010 Dec; 29(6):E7.
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Yousefzadeh DK. Neonatal and pediatric sonography. Curr Opin Radiol. 1992 Apr; 4(2):111-25.
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