2026-07-21T16:29:11Zhttps://repisalud.isciii.es/rest/oai/request

oai:repisalud.isciii.es:20.500.12105/140602025-03-12T09:51:12Zcom_20.500.12105_5571com_20.500.12105_2404com_20.500.12105_2403col_20.500.12105_5713

00925njm 22002777a 4500 dc Esteban-Marfil, MV author Martínez-Espinosa, N author Santiago-Gutiérrez, C author Sierra-Córcoles, C author Cruz-Moreno, J de la author Sanchís-Calvo, A author Crow, YJ author Martínez-Frías, María Luisa author 2009-10 Aicardi-Goutières Syndrome (AGS) is a genetic disorder with autosomal recessive aetiology characterized by an early developed encephalopathy with severe physical and mental handicaps. The neonatal form (20% of the cases) shows a phenotype similar to a congenital infection, hence there exists the possibility of misdiagnosis and misinformation to parents about the risk of recurrence. We present a new case of AGS with a neonatal onset and also review clinical patterns, laboratory and neuroimaging findings, and new advances in geneticmolecular diagnosis that have allowed us to delineate the phenotypic spectrum and confirm the aetiology in more than 80% of cases. Boletín del ECEMC: Rev Dismor Epidemiol 2009; V (nº 8): 2-8 0210–3893 Boletín del ECEMC: Revista de Dismorfología y Epidemiología http://hdl.handle.net/20.500.12105/14060 Síndrome de Aicardi-Goutieres de presentación neonatal simulando infección congénita