Chiari malformation type I: related conditions

被引:13
|
作者
deSouza, Ruth-Mary [2 ]
Zador, Zsolt [3 ]
Frim, David M. [1 ]
机构
[1] Univ Chicago, Neurosurg Sect, Chicago, IL 60637 USA
[2] Univ Hosp, Dept Surg, Coventry, W Midlands, England
[3] Good Hope Hosp, Dept Acute Med, Sutton Coalfield, England
关键词
Chiari malformation etiology; Genetic overlap; Multi-system manifestation; GROWTH-HORMONE DEFICIENCY; FORAMEN MAGNUM DECOMPRESSION; NERVOUS-SYSTEM MALFORMATIONS; POSTERIOR CRANIAL FOSSA; CRANIOMETAPHYSEAL DYSPLASIA; NEUROFIBROMATOSIS TYPE-1; PSEUDOTUMOR CEREBRI; SUDDEN-DEATH; PEDIATRIC POPULATION; UNUSUAL ASSOCIATION;
D O I
10.1179/016164111X12962202723922
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chiari malformation type I (CMI) is a morphological diagnosis defined as the inferior displacement of the cerebellum through the foramen magnum. In parallel to this basic definition of CMI, there are diagnoses that co-exist with CMI in selected patients. In addition, there are specific constellations of clinical symptoms and signs reported in the literature that occur non-randomly in patients affected by CMI. There is no established system that categorizes these CMI-related conditions or even defines them as causes or consequences of CMI. Identifying the relationship between CMI and these associated disorders may allow greater understanding of CMI etiology and potentially inform CMI management.
引用
收藏
页码:278 / 284
页数:7
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