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Research ArticlePediatric Neuroimaging
Open Access

Neuroradiologic Features of CASK Mutations

J. Takanashi, H. Arai, S. Nabatame, S. Hirai, S. Hayashi, J. Inazawa, N. Okamoto and A.J. Barkovich
American Journal of Neuroradiology October 2010, 31 (9) 1619-1622; DOI: https://doi.org/10.3174/ajnr.A2173
J. Takanashi
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H. Arai
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S. Nabatame
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S. Hirai
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S. Hayashi
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J. Inazawa
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N. Okamoto
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A.J. Barkovich
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Abstract

SUMMARY: Mutations of the CASK gene are associated with X-linked mental retardation with microcephaly and disproportionate brain stem and cerebellar hypoplasia in females. The areas of the cerebrum, corpus callosum, pons, midbrain, and cerebellar vermis and hemisphere and a ratio of cerebrum/corpus callosum areas were measured in 5 female patients with CASK mutations, 67 female controls, and 5 patients with pontine hypoplasia. MR imaging in patients with CASK mutations revealed a normal size of the corpus callosum and a low ratio of the cerebrum/corpus callosum with a reduced area of the cerebrum, pons, midbrain, and cerebellar vermis and hemispheres. The 5 patients with pontine hypoplasia showed thinning of the corpus callosum and a high ratio of the cerebrum/corpus callosum, irrespective of the size of the cerebrum. The normal size of the corpus callosum, which gives an impression of callosal thickening at first glance, may be an imaging clue to detect patients with CASK mutations.

Abbreviations

CASK
calcium/calmodulin-dependent serine protein kinase
CINAP
CASK interacting nucleosome assembly protein
PEHO
progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy
TBR1
T-brain-1
RELN
reelin
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American Journal of Neuroradiology: 31 (9)
American Journal of Neuroradiology
Vol. 31, Issue 9
1 Oct 2010
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Cite this article
J. Takanashi, H. Arai, S. Nabatame, S. Hirai, S. Hayashi, J. Inazawa, N. Okamoto, A.J. Barkovich
Neuroradiologic Features of CASK Mutations
American Journal of Neuroradiology Oct 2010, 31 (9) 1619-1622; DOI: 10.3174/ajnr.A2173

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Neuroradiologic Features of CASK Mutations
J. Takanashi, H. Arai, S. Nabatame, S. Hirai, S. Hayashi, J. Inazawa, N. Okamoto, A.J. Barkovich
American Journal of Neuroradiology Oct 2010, 31 (9) 1619-1622; DOI: 10.3174/ajnr.A2173
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Cited By...

  • Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein
  • Complete loss of the X-linked gene CASK causes severe cerebellar degeneration
  • Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study
  • Complete loss of CASK causes severe ataxia through cerebellar degeneration in human and mouse
  • Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution
  • Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI
  • Phenotypic spectrum associated with CASK loss-of-function mutations
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