Late-onset Aicardi Goutières syndrome: a characterization of presenting clinical features

INTRODUCTION: Aicardi Goutières Syndrome (AGS) is a genetic interferonopathy characterized by early onset of severe neurologic injury with intracranial calcifications, leukoencephalopathy, and systemic inflammation. Increasingly, a spectrum of neurologic dysfunction and presentation beyond the infan...

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Vydáno v:Pediatr Neurol
Hlavní autoři: Piccoli, Cara, Bronner, Nowa, Gavazzi, Francesco, Dubbs, Holly, De Simone, Micaela, De Giorgis, Valentina, Orcesi, Simona, Fazzi, Elisa, Galli, Jessica, Masnada, Silvia, Tonduti, Davide, Varesio, Costanza, Vanderver, Adeline, Vossough, Arastoo, Adang, Laura
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7856674/
https://ncbi.nlm.nih.gov/pubmed/33307271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2020.10.012
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