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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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Bibliografiska uppgifter
I publikationen:J Pediatr Neurosci
Huvudupphovsmän: Alkan, Gülsüm, Emiroglu, Melike Keser, Kartal, Ayse
Materialtyp: Artigo
Språk:Inglês
Publicerad: Medknow Publications & Media Pvt Ltd 2017
Ämnen:
Länkar: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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