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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Detalles Bibliográficos
Autores principales: Maldjian, Pierre, Sanders, Alison Esteva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801571/
https://www.ncbi.nlm.nih.gov/pubmed/29441224
http://dx.doi.org/10.4103/jcis.JCIS_66_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801571/
https://www.ncbi.nlm.nih.gov/pubmed/29441224
http://dx.doi.org/10.4103/jcis.JCIS_66_17

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