DiGeorge Syndrome with Sacral Myelomeningocele and Epilepsy

DiGeorge syndrome (DGS) is the most common microdeletion syndrome. The phenotype of DGS is highly variable involving facial, velopharyngeal, cardiac, immunologic, endocrinal, and neuropsychiatric abnormalities. Although neural tube defects (NTDs) have not been described as components of DGS in stand...

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Detalles Bibliográficos
Autores principales: Alkan, Gülsüm, Emiroglu, Melike Keser, Kartal, Ayse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890554/
https://www.ncbi.nlm.nih.gov/pubmed/29675073
http://dx.doi.org/10.4103/jpn.JPN_92_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890554/
https://www.ncbi.nlm.nih.gov/pubmed/29675073
http://dx.doi.org/10.4103/jpn.JPN_92_17

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