Spastic paraparesis and marked improvement of leukoencephalopathy in Aicardi-Goutières syndrome.
Neuropediatrics
; 45(6): 406-10, 2014 Dec.
Article
em En
| MEDLINE
| ID: mdl-25343331
ABSTRACT
Aicardi-Goutières syndrome (AGS) is a rare genetic disorder with inflammatory immune-mediated pathogenesis. Disease onset is most commonly marked by recurrent fevers, irritability, and developmental regression in the 1st year of life. A stable phase characterized by severe spastic quadriparesis and cognitive deficit follows. Brain calcifications, leukoencephalopathy, and cerebral atrophy are the radiological hallmarks of AGS and often show progression over time. We present an atypical patient with late-onset AGS characterized by spastic paraparesis and a leukoencephalopathy that markedly improved during follow-up, demonstrating a nonprogressive disease course and the exceptional amelioration of the white matter abnormalities.
Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Doenças Autoimunes do Sistema Nervoso
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Paraparesia Espástica
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Leucoencefalopatias
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Malformações do Sistema Nervoso
Limite:
Child
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Female
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Humans
Idioma:
En
Ano de publicação:
2014
Tipo de documento:
Article