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Case Report: Beckwith-Wiedemann syndrome with congenital heart disease

2023-11-27

Abstract excerpt

<h4>Background: </h4> Beckwith-Wiedemann syndrome (BWS) is caused by a genetic mutation of chromosome defects at 11p15 S. It is seen in 1 in 10,400 to 13,800 cases, and the association between BWS and congenital heart disease (CHD) is not reported; amniocentesis or chorionic villus sampling is a diagnostic tool. Tongue reduction surgery for macroglossia is the treatment of choice. An early psychological assessment...

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Literature Corpus work: ce36e2f9-1be6-5ac1-b2d8-968b8a60e22d
DOI: 10.12688/f1000research.141829.1

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