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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
Ataxia-telangiectasia, an autosomal recessive disorder caused by defect of the ataxia-telangiectasia mutated gene, is characterized by progressive neurologic impairment with cerebellar atrophy, ocular and cutaneous telangiectasia, immunodeficiency, heightened sensitivity to ionizing radiation and su...
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| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society of Neuroradiology
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4106125/ https://ncbi.nlm.nih.gov/pubmed/23886747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A3646 |
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