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
|
| MeSH Number(s) |
C16.131.077.133 C16.131.260.080 C16.320.180.080
|
| 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
|
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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 1996 | 0 | 1 | 1 |
| 1997 | 3 | 0 | 3 |
| 1998 | 0 | 1 | 1 |
| 1999 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2005 | 3 | 0 | 3 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 2 | 1 | 3 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 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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Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children. Cancer. 2024 02 01; 130(3):467-475.
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Improving the prenatal diagnosis of Beckwith-Wiedemann syndrome. Prenat Diagn. 2021 06; 41(7):795-797.
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Surgical Outcomes of Patients with Beckwith-Wiedemann Syndrome. J Pediatr Surg. 2018 May; 53(5):1042-1045.
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TGF-?/?2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome. J Clin Invest. 2016 Feb; 126(2):527-42.
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Hepatoblastoma in children with Beckwith-Wiedemann syndrome: does it warrant different treatment? J Pediatr Hematol Oncol. 2014 Jul; 36(5):369-73.
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Giant breast tumors in a patient with Beckwith-Wiedemann syndrome. Am J Med Genet A. 2014 Jan; 164A(1):182-5.
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Recurrent hemangioendothelioma in a pediatric patient: report and review of the literature. J Pediatr Surg. 2013 Jun; 48(6):1426-8.
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Endocrine tumors associated with neurofibromatosis type 1, Peutz-Jeghers syndrome and other familial neoplasia syndromes. Front Horm Res. 2013; 41:166-81.
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Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome. Am J Med Genet A. 2012 Oct; 158A(10):2534-6.
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Epigenetic silencing of beta-spectrin, a TGF-beta signaling/scaffolding protein in a human cancer stem cell disorder: Beckwith-Wiedemann syndrome. J Biol Chem. 2010 Nov 12; 285(46):36112-20.