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MeSH Tree Location(s) for Beckwith-Wiedemann Syndrome

Scope Note:
A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities.

Förklaring:
Ett syndrom kännetecknat av multipla defekter, främst navelbråck, makroglossi och gigantism, men även visceromegali, hypoglycemi, öronabnormaliteter osv.

See also: Gigantism


Location corresponding to Mesh Number C16.131.077.133

Abnormalities, Multiple  Missbildningar, multipla
Beckwith-Wiedemann Syndrome   Beckwith-Wiedemanns syndrom
BWS
EMG syndrom
Location corresponding to Mesh Number C16.131.260.080

Chromosome Disorders  Kromosomrubbningar
Beckwith-Wiedemann Syndrome   Beckwith-Wiedemanns syndrom
BWS
EMG syndrom
Location corresponding to Mesh Number C16.320.180.080

Chromosome Disorders  Kromosomrubbningar
Beckwith-Wiedemann Syndrome   Beckwith-Wiedemanns syndrom
BWS
EMG syndrom
MeSH Start Page
© Karolinska Institutet University Library 1998. Last modified 2013-01-31.