American Journal of Neuroradiology · 2007 · 148 citations · 23 references
MedicineNeuroscienceRadiologyDiagnostic ImagingDiagnostic RadiologyNeuroradiologyBrain ImagingCerebellar AnatomyDiffusion ImagingMagnetic Resonance ImagingMedical ImagingNeurogenetic DisordersDiffusion Magnetic Resonance ImagingDiffusion MapsFractional AnisotropyPyramidal TractStructural NeuroimagingSuperior Cerebellar PeduncleT1-weighted ImagingT2-weighted Imaging
BACKGROUND AND PURPOSE: Neuropathologic findings and preliminary imaging studies demonstrated the absence of pyramidal tract and superior cerebellar peduncular decussation in individual patients with Joubert syndrome (JS). We hypothesized that functional-structural neuroimaging findings do not differ between the genetic forms of JS. MATERIALS AND METHODS: MR imaging was performed with a 3T MR imaging-unit. Multiplanar T2- and T1-weighted imaging was followed by diffusion tensor imaging (DTI). Isotropic diffusion-weighted images, apparent diffusion coefficient maps, and color-coded fractional anisotropy maps, including tractography, were subsequently calculated. RESULTS: In all 6 patients studied, DTI showed that the fibers of the superior cerebellar peduncles did not decussate in the mesencephalon and the corticospinal tract failed to cross in the caudal medulla. The patients represented various genetic forms of JS. CONCLUSION: In JS, the fibers of the pyramidal tract and the superior cerebellar peduncles do not cross, irrespective of the underlying mutation.
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Familial agenesis of the cerebellar vermis
Marie Joubert, Jean-Jacques Eisenring, Jennifer Preston et al. · Neurology · 1969 · 651 citations · Full text
Medicine, Neurology, Pediatrics +10