Literature DB >> 8423872

The use of magnetic resonance imaging in diagnosing infantile neuroaxonal dystrophy.

Y Tanabe1, M Iai, M Ishii, K Tamai, T Maemoto, K Ooe, S Takashima.   

Abstract

We used MRI to investigate the brains of four children ranging from 3 to 10 years of age with infantile neuroaxonal dystrophy. T2-weighted imaging revealed characteristic findings of marked cerebellar atrophy and diffuse hyperintensity of the cerebellar cortex. At autopsy, one child had extensive astrogliosis and neuronal loss with shrinkage of the cerebellar cortex, in addition to typical widespread changes of neuroaxonal dystrophy. The characteristic hyperintensity of the cerebellar cortex on T2-weighted imaging probably is secondary to the extensive gliosis and shrinkage of the cerebellar cortex. These cerebellar findings on MRI may permit early diagnosis of infantile neuroaxonal dystrophy.

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Year:  1993        PMID: 8423872     DOI: 10.1212/wnl.43.1_part_1.110

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy.

Authors:  Yongyi Zou; Haiyan Luo; Huizhen Yuan; Kang Xie; Yan Yang; Shuhui Huang; Bicheng Yang; Yanqiu Liu
Journal:  Front Neurol       Date:  2022-07-06       Impact factor: 4.086

Review 2.  Clinical and genetic delineation of neurodegeneration with brain iron accumulation.

Authors:  A Gregory; B J Polster; S J Hayflick
Journal:  J Med Genet       Date:  2008-11-03       Impact factor: 6.318

3.  Genetic ablation of PLA2G6 in mice leads to cerebellar atrophy characterized by Purkinje cell loss and glial cell activation.

Authors:  Zhengshan Zhao; Jing Wang; Chunying Zhao; Weina Bi; Zhenyu Yue; Zhongmin Alex Ma
Journal:  PLoS One       Date:  2011-10-28       Impact factor: 3.240

  3 in total

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