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Orphanet J Rare Dis ; 11(1): 169, 2016 12 07.
Artigo em Inglês | MEDLINE | ID: mdl-27927234

RESUMO

BACKGROUND: Canavan disease is a devastating autosomal recessive leukodystrophy leading to spongiform degeneration of the white matter. There is no cure or treatment for Canavan disease, and disease progression is poorly understood. RESULTS: We report a new presentation of a patient found to have Canavan disease; brain magnetic resonance imaging (MRI) revealed white matter cytotoxic edema, indicative of an acute active destructive process. We performed a comprehensive review of published cases of Canavan disease reporting brain MRI findings, and found that cytotoxic brain edema is frequently reported in early Canavan disease. CONCLUSIONS: Our results and the literature review support the notion of an acute phase in Canavan disease progression. These findings suggest that there is a window available for therapeutic intervention and support the need for early identification of patients with Canavan disease.


Assuntos
Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Doença de Canavan/diagnóstico por imagem , Doença de Canavan/patologia , Biomarcadores , Humanos
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