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The Aircardi-Goutières syndrome: variable clinical expression in two siblings
A Verrips1, J A Hiel, F J Gabreëls
1Department of Pediatric Neurology, University Hospital Nijmegen, The Netherlands.
Abstract:
We report 2 siblings with the Aicardi-Goutières syndrome (encephalopathy, basal ganglia calcifications, and persistent cerebrospinal fluid pleiocytosis). The eldest sibling is severely retarded; his younger brother has only mild, slowly progressive neurological deficits. To our knowledge, such a striking difference in clinical expression has not been reported previously.
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