Relapsing–remitting clinical course expands the phenotype of Aicardi–Goutières syndrome

Aicardi–Goutières syndrome (AGS) is a rare and likely underdiagnosed genetic leukoencephalopathy, typically presenting in infancy with encephalopathy and characteristic neuroimaging features, with residual static neurological deficits. We describe a patient who, following an initial presentation at...

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Detalles Bibliográficos
Autores principales: Lambe, Jeffrey, Murphy, Olwen C., Mu, Weiyi, Sondergaard Schatz, Krista, Barañano, Kristin W., Venkatesan, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034496/
https://www.ncbi.nlm.nih.gov/pubmed/31920009
http://dx.doi.org/10.1002/acn3.50979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034496/
https://www.ncbi.nlm.nih.gov/pubmed/31920009
http://dx.doi.org/10.1002/acn3.50979

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