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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART): Table 1

1 Jan 2003

Abstract excerpt

Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from mutations or epimutations affecting imprinted genes on chromosome 11p15.5.1 The classical clinical features of BWS are macroglossia, pre- and/or postnatal overgrowth, and anterior abdominal wall defects (umbilical hernia or exomphalos). Additional more variable features include hemihypertrophy, neonatal hypoglycaemia, facial naevus...

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Share to Epigenetics and DNA Methylation
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PMID: 12525545
DOI: 10.1136/jmg.40.1.62

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