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General approach to velocardiofacial anomalies: a pediatric case presenting with Fallot tetralogy
Velocardiofacial syndrome (VCFS), also known as “Shprintzen syndrome” or “22q11.2 deletion syndrome” is an autosomal dominant genetic disorder with a wide range of phenotypical findings. It is majorly characterized by cleft palate, dysmorphic face, conotruncal cardiac anomalies, growth retardation,...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Kare Publishing
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175041/ https://www.ncbi.nlm.nih.gov/pubmed/28058329 http://dx.doi.org/10.14744/nci.2014.04695 |