Waardenburg Syndrome and Left Persistent Superior Vena Cava

Waardenburg syndrome (WS) is a rare genetic disorder secondary to neural crest cell developmental abnormalities. It is predominantly described as an auditory–pigmentary syndrome with diverse patient presentation, typically involving congenital sensorineural hearing loss and pigmentation abnormalitie...

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Detalles Bibliográficos
Autores principales: Raissi, Driss, Christie, Alexander, Applegate, Kimberly
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/PMC6251238/
https://www.ncbi.nlm.nih.gov/pubmed/30546928
http://dx.doi.org/10.4103/jcis.JCIS_31_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251238/
https://www.ncbi.nlm.nih.gov/pubmed/30546928
http://dx.doi.org/10.4103/jcis.JCIS_31_18

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