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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Chromosome Disorders > Beckwith-Wiedemann Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Chromosome Disorders > Beckwith-Wiedemann Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Beckwith-Wiedemann Syndrome

Terme préférentiel

Beckwith-Wiedemann Syndrome  

Type

  • mesh:Descriptor

Définition

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

Concept générique

Concepts associés

Synonyme(s)

  • EMG Syndrome
  • Exomphalos-Macroglossia-Gigantism Syndrome
  • Wiedemann-Beckwith Syndrome
  • Wiedemann-Beckwith Syndrome (WBS)
  • Wiedemann Syndrome

Qualificatif(s) autorisé(s)

Traductions

  • Syndrome de Beckwith-Wiedemann

    français

  • Omphalocèle-macroglossie-gigantisme
  • SBW (Syndrome de Beckwith-Wiedemann)
  • SWB (Syndrome de Wiedemann-Beckwith)
  • Syndrome d'hypertrophie staturale avec macroglossie et omphalocèle
  • Syndrome de Wiedemann-Beckwith
  • Syndrome omphalocèle-macroglossie-gigantisme

URI

http://data.loterre.fr/ark:/67375/JVR-LLFZ7FD5-V

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RDF/XML TURTLE JSON-LD Date de création 26/04/1982, dernière modification le 12/05/2021