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Beckwith-Wiedemann syndrome is a genetic disorder linked to genetic imprinting and characterized by overgrowth and increased cancer risk.
Beckwith-Wiedemann syndrome is a genetic disorder often attributed to genetic imprinting, where certain genes are expressed based on their parental origin. This syndrome is characterized by overgrowth, abdominal wall defects, and an increased risk of certain childhood cancers. Additionally, other syndromes like Prader-Willi and Angelman syndrome are also linked to abnormalities in chromosome 15 due to genetic imprinting.
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