 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
- Exomphalos-Macroglossia-Gigantism Syndrome
- Wiedemann-Beckwith Syndrome (WBS)
- Syndrome, Wiedemann-Beckwith (WBS)
- Syndromes, Wiedemann-Beckwith (WBS)
- Wiedemann Beckwith Syndrome (WBS)
- Wiedemann-Beckwith Syndromes (WBS)
- EMG Syndrome
- EMG Syndromes
- Syndrome, EMG
- Syndromes, EMG
- Wiedemann-Beckwith Syndrome
- Syndrome, Wiedemann-Beckwith
- Wiedemann Beckwith Syndrome
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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 |
|---|
| 1999 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2008 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Beckwith-Wiedemann Syndrome" by people in Profiles.
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Khoshnam N, Robinson H, Clay MR, Schaffer LR, Gillespie SE, Shehata BM. Calcifying nested stromal-epithelial tumor (CNSET) of the liver in Beckwith-Wiedemann syndrome. Eur J Med Genet. 2017 Feb; 60(2):136-139.
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Alsultan A, Lovell MA, Hayes KL, Allshouse MJ, Garrington TP. Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome. Pediatr Blood Cancer. 2008 Nov; 51(5):695-8.
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Jackson EM, Shaikh TH, Zhang F, Wainwright LM, Storm PB, Hakonarson H, Zackai EH, Biegel JA. Atypical teratoid/rhabdoid tumor in a patient with Beckwith-Wiedemann syndrome. Am J Med Genet A. 2007 Aug 01; 143A(15):1767-70.
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Borer JG, Kaefer M, Barnewolt CE, Elias ER, Hobbs N, Retik AB, Peters CA. Renal findings on radiological followup of patients with Beckwith-Wiedemann syndrome. J Urol. 1999 Jan; 161(1):235-9.
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Spritz RA, Mager D, Pauli RM, Laxova R. Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome. Am J Hum Genet. 1986 Aug; 39(2):265-73.
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