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22q11 Deletion Syndrome with Vascular Anomalies
DiGeorge syndrome, also termed 22q11.2 deletion syndrome, represents a spectrum of disorders that include thymic aplasia/hypoplasia, parathyroid aplasia/hypoplasia, conotruncal vascular anomalies, and velocardiofacial (Shprintzen) syndrome. This case report describes a novel constellation of cardiov...
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| Publicado no: | J Clin Imaging Sci |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5801571/ https://ncbi.nlm.nih.gov/pubmed/29441224 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jcis.JCIS_66_17 |
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