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.

Also Known As:

Exomphalos Macroglossia Gigantism Syndrome; Syndrome, Exomphalos-Macroglossia-Gigantism; EMG Syndrome; Exomphalos-Macroglossia-Gigantism Syndrome; Beckwith Wiedemann Syndrome; EMG Syndromes; Exomphalos-Macroglossia-Gigantism Syndromes; Syndrome, Beckwith-Wiedemann; Syndrome, EMG; Syndrome, Wiedemann; Syndrome, Wiedemann-Beckwith; Syndrome, Wiedemann-Beckwith (WBS); Wiedemann Beckwith Syndrome; Wiedemann Beckwith Syndrome (WBS); Wiedemann Syndromes; Wiedemann-Beckwith Syndromes (WBS); Wiedemann Syndrome; Wiedemann-Beckwith Syndrome; Wiedemann-Beckwith Syndrome (WBS)

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Multiple Abnormalities: 213
    - Beckwith-Wiedemann Syndrome: 218
  - Chromosome Disorders: 140
    - Beckwith-Wiedemann Syndrome: 218
- Inborn Genetic Diseases: 12342
  - Chromosome Disorders: 140
    - Beckwith-Wiedemann Syndrome: 218
  - Imprinting Disorders: 66
    - Beckwith-Wiedemann Syndrome: 218

Fabienne Arcin-Thoury Selected Research

Fabienne Arcin-Thoury Research Topics

Disease

Drug/Important Bio-Agent (IBA)