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MRI diagnosis of infantile Alexander disease in a 14 month old African boy
Alexander disease, also known as fibrinoid leukodystrophy, is a rare leukoencephalopathy which occurs due to a mutation in the glial fibrillary acid protein (GFAP) gene. Magnetic resonance imaging (MRI) has proven to be highly sensitive in making the diagnosis. Typical MRI findings, in combination w...
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| Publicado no: | J Radiol Case Rep |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
EduRad
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5443584/ https://ncbi.nlm.nih.gov/pubmed/28580052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3941/jrcr.v10i10.2943 |
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