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Beckwith-Wiedemann Syndrome
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Definition
: A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.
See Also
Gigantism
;
Silver-Russell Syndrome
Other names
Wiedemann-
Beckwith Syndrome (WBS); Wiedemann-
Beckwith Syndrome; Exomphalos-
Macroglossia-
Gigantism Syndrome; Wiedemann-
Beckwith Syndromes (WBS); Wiedemann Beckwith Syndrome (WBS); Wiedemann Beckwith Syndrome; Syndromes, Wiedemann-
Beckwith (WBS); Syndromes, Exomphalos-
Macroglossia-
Gigantism; Syndrome, Wiedemann-
Beckwith (WBS); Syndrome, Wiedemann-
Beckwith; Syndrome, Exomphalos-
Macroglossia-
Gigantism; Syndrome, Beckwith-
Wiedemann; Exomphalos-
Macroglossia-
Gigantism Syndromes; Exomphalos Macroglossia Gigantism Syndrome; Beckwith Wiedemann Syndrome
Substance
CAS Registry & name
Categories
Source
Franceschini Vardeu Guala syndrome
0
*Beckwith-Wiedemann Syndrome.
Am J Med Genet. 1993;46(3):353-4
LIT1 RNA
0
*RNA, Untranslated
Beckwith-Wiedemann Syndrome.
Am J Hum Genet 2002 Mar;70(3):604-11
SLC22A18AS protein, human
0
*Membrane Proteins
Beckwith-Wiedemann Syndrome
RNA, Antisense.
Genomics 1998 Apr 1;49(1):38-51