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Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia
Alexander disease (AxD) is a rare autosomal dominant leukodystrophy with three clinical subtypes: infantile, juvenile and adult. Forms differ by age of symptoms occurrence and the clinical presentation. Although recent data suggest considering only two subtypes: type I (infantile onset with lesions...
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| Udgivet i: | Balkan J Med Genet |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Sciendo
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6956636/ https://ncbi.nlm.nih.gov/pubmed/31942421 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/bjmg-2019-0017 |
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