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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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 2 | 1 | 3 |
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Below are the most recent publications written about "Beckwith-Wiedemann Syndrome" by people in Profiles.
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Why scientists with children who have disabilities need a different career trajectory. Nature. 2020 07; 583(7817):646.
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Case Report of Infant With Features of Beckwith-Wiedemann Syndrome Diagnosed With Genome-wide Uniparental Disomy. S D Med. 2017 Nov; 70(11):505-509.
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Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases. BMC Med Genet. 2017 10 18; 18(1):115.
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Fateful imprints. Science. 2017 Jan 13; 355(6321):122-125.