Beckwith-Wiedemann Syndrome
A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.
Year introduced: 1983
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Subheadings:
Tree Number(s): C16.131.077.133, C16.131.260.080, C16.320.180.080, C16.320.447.375
MeSH Unique ID: D001506
Entry Terms:
- Beckwith Wiedemann Syndrome
- Syndrome, Beckwith-Wiedemann
- EMG Syndrome
- EMG Syndromes
- Syndrome, EMG
- Exomphalos-Macroglossia-Gigantism Syndrome
- Exomphalos Macroglossia Gigantism Syndrome
- Exomphalos-Macroglossia-Gigantism Syndromes
- Syndrome, Exomphalos-Macroglossia-Gigantism
- Wiedemann-Beckwith Syndrome
- Syndrome, Wiedemann-Beckwith
- Wiedemann Beckwith Syndrome
- Wiedemann-Beckwith Syndrome (WBS)
- Syndrome, Wiedemann-Beckwith (WBS)
- Wiedemann-Beckwith Syndromes (WBS)
- Wiedemann Beckwith Syndrome (WBS)
- Wiedemann Syndrome
- Syndrome, Wiedemann
- Wiedemann Syndromes
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