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Up to: Hereditary neoplastic syndrome · Familial hypertrophic cardiomyopathy · Overgrowth syndrome

Beckwith-Wiedemann syndrome

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations.

6 trials tagged with this condition →

Beckwith-Wiedemann syndrome due to 11p15 microdeletion 0 trials
Beckwith-Wiedemann syndrome due to 11p15 microduplication 0 trials
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion 0 trials
Beckwith-Wiedemann syndrome due to CDKN1C mutation 0 trials
Beckwith-Wiedemann syndrome due to NSD1 mutation 0 trials
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 0 trials
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 0 trials
Franceschini Vardeu Guala syndrome 0 trials