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Recurrent Encephalopathy with Spinal Cord Involvement: An Atypical Manifestation of Aicardi–Goutières Syndrome
Aicardi–Goutières syndrome (AGS) is a rare, genetic inflammatory disease due to mutations in any of the seven genes discovered to date (TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1). Clinical onset is seen most commonly in utero or in infancy; irritability, feeding difficulties, jitt...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327704/ https://www.ncbi.nlm.nih.gov/pubmed/30692772 http://dx.doi.org/10.4103/aian.AIAN_12_18 |