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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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| Vydáno v: | J Pediatr Neurosci |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5890554/ https://ncbi.nlm.nih.gov/pubmed/29675073 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jpn.JPN_92_17 |
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