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A Case of Infantile Alexander Disease Accompanied by Infantile Spasms Diagnosed by DNA Analysis
Alexander disease (AD) is a rare leukodystrophy of the central nervous system of unknown etiology. AD is characterized by progressive failure of central myelination and the accumulation of Rosenthal fibers in astrocytes, and is inevitably lethal in nature. Symptomatically, AD is associated with leuk...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722014/ https://www.ncbi.nlm.nih.gov/pubmed/17043438 http://dx.doi.org/10.3346/jkms.2006.21.5.954 |