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| Type Ⅱ Alexander disease in preschool children: report of one case |
| ZHANG Yin-xia, LIU Jia-ying, ZHANG Chen-ying, AN Peng, GAO Si-jia |
| Department of Radiology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China |
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[2]臧莉莉，吴哗，王静敏，等． 亚历山大病12例中国患儿临床及遗传学研究[J]． 中华儿科杂志，2012，50（5）：371-375．
[3]Prust M, Wang J, Morizono H, et al． GFAP mutations, age at onset, and clinical subtypes in Alexander disease[J]. Neurology, 2011, 77(13): 1287-1294．
[4]Kyllerman M, Rosengren L, Wiklund LM, et al. Increased levels of GFAP in the cerebrospinal fluid in three subtypes of genetically confirmed Alexander disease[J]. Ncuropediatrics, 2005, 36(5): 319-323.
[5]Garcia-Reitboeck P, Mackinnun AD, Mcentagart M, et al． Prominent cognitive decline and behavioural disturbance in late-onset Alexander disease[J]． J Neurol Sci, 2015, 357(1-2): 319-321.
[6]夏晓娜，董影，叶春涛，等. 亚历山大病一例[J]. 临床放射学杂志，2016，35（10）：1540-1541.
[7]Tschampa HJ, Greschus S, Vinahl M, el al. MS-like presentation of Alexander disease with multifocal lesions and oligoclonal bands[J]. J Neurol, 2011, 258(5): 935-937.
[8]班婷婷，吴晔，张仲斌，等. 亚历山大病Ⅱ型4例临床及文献复习[J]. 中华实用儿科临床杂志，2016，31（9）：700-705. |
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