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Title: The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patients. Author: Lanzi G, Fazzi E, D'Arrigo S, Orcesi S, Maraucci I, Uggetti C, Bertini E, Lebon P. Journal: Neurology; 2005 May 10; 64(9):1621-4. PubMed ID: 15883328. Abstract: Described are the outcomes of 11 Italian patients with Aicardi-Goutières syndrome. Neurologic symptoms progressed in the first year of life and stabilized by the end of the second year in 10 patients. White matter abnormalities remained stable; cerebral atrophy was stable in four patients and progressive in two. Calcifications increased (in number and size) in two of six patients. Serial CSF and serum interferon-alpha measurements (three patients) showed reduced CSF interferon-alpha levels.[Abstract] [Full Text] [Related] [New Search]