Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics

被引:87
作者
Doherty, Dan [1 ]
Millen, Kathleen J. [1 ]
Barkovich, A. James [2 ]
机构
[1] Univ Washington, Seattle Childrens Res Inst, Ctr Integrat Brain Res, Div Genet Med,Dept Pediat, Seattle, WA 98195 USA
[2] Univ Calif San Francisco, Dept Radiol & Biomol Imaging, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
DANDY-WALKER MALFORMATION; TEGMENTAL CAP DYSPLASIA; CAUSE PONTOCEREBELLAR HYPOPLASIA; NEURONAL MIGRATION; CEREBELLAR DEVELOPMENT; MUTATIONS CAUSE; BRAIN-STEM; MUSCULAR-DYSTROPHIES; CONGENITAL FIBROSIS; MOUSE MODEL;
D O I
10.1016/S1474-4422(13)70024-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Historically, the midbrain and hindbrain have been considered of secondary importance to the cerebrum, which has typically been acknowledged as the most important part of the brain. In the past, radiologists and pathologists did not regularly examine these structures-also known as the brainstem and cerebellum-because they are small and difficult to remove without damage. With recent developments in neuroimaging, neuropathology, and neurogenetics, many developmental disorders of the midbrain and hindbrain have emerged as causes of neurodevelopmental dysfunction. These research advances may change the way in which we treat these patients in the future and will enhance the clinical acumen of the practising neurologist and thereby improve the diagnosis and treatment of these patients.
引用
收藏
页码:381 / 393
页数:13
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