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Research ArticlePediatric Neuroimaging

Interpeduncular Heterotopia in Joubert Syndrome: A Previously Undescribed MR Finding

I. Harting, U. Kotzaeridou, A. Poretti, A. Seitz, J. Pietz, M. Bendszus and E. Boltshauser
American Journal of Neuroradiology June 2011, DOI: https://doi.org/10.3174/ajnr.A2488
I. Harting
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U. Kotzaeridou
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A. Poretti
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A. Seitz
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J. Pietz
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M. Bendszus
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E. Boltshauser
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Abstract

SUMMARY: The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most often autosomal-recessive disorder with a characteristic malformation of the midhindbrain. We describe 3 patients with JSRD and the additional MR finding of tissue resembling heterotopia in the interpeduncular fossa, which in one patient was combined with a more extensive intramesencephalic heterotopia. Interpeduncular heterotopia has not been reported previously, either in the context of JSRD or as a separate entity. This new imaging feature enlarges the spectrum of brain stem abnormalities in JSRD. In view of the underlying ciliopathy, it seems likely that the interpeduncular heterotopia results from misdirected migration.

Footnotes

  • CNS
    central nervous system
    GE
    gradient-echo
    JSRD
    Joubert syndrome and related disorders
    T1WI
    T1-weighted imaging
    T2WI
    T2-weighted imaging

  • © 2011 American Society of Neuroradiology
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Cite this article
I. Harting, U. Kotzaeridou, A. Poretti, A. Seitz, J. Pietz, M. Bendszus, E. Boltshauser
Interpeduncular Heterotopia in Joubert Syndrome: A Previously Undescribed MR Finding
American Journal of Neuroradiology Jun 2011, DOI: 10.3174/ajnr.A2488

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Interpeduncular Heterotopia in Joubert Syndrome: A Previously Undescribed MR Finding
I. Harting, U. Kotzaeridou, A. Poretti, A. Seitz, J. Pietz, M. Bendszus, E. Boltshauser
American Journal of Neuroradiology Jun 2011, DOI: 10.3174/ajnr.A2488
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