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Case ReportPediatricsC

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 August 2011, 32 (7) 1286-1289; 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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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.

Abbreviations

CNS
central nervous system
GE
gradient-echo
JSRD
Joubert syndrome and related disorders
T1WI
T1-weighted imaging
T2WI
T2-weighted imaging
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American Journal of Neuroradiology: 32 (7)
American Journal of Neuroradiology
Vol. 32, Issue 7
1 Aug 2011
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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 Aug 2011, 32 (7) 1286-1289; 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 Aug 2011, 32 (7) 1286-1289; DOI: 10.3174/ajnr.A2488
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