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Williams-Beuren's Syndrome: A Case Report
Williams-Beuren syndrome is a rare familial multisystem disorder occurring in 1 per 20,000 live births. It is characterized by congenital heart defects (CHD), skeletal and renal anomalies, cognitive disorder, social personality disorder and dysmorphic facies. We present a case of Williams syndrome t...
Autores principales: | Zamani, Hassan, Babazadeh, Kazem, Fattahi, Saeid, Mokhtari-Esbuie, Farzad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425039/ https://www.ncbi.nlm.nih.gov/pubmed/22927862 http://dx.doi.org/10.1155/2012/585726 |
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