Magnetic resonance imaging of the brain showed generalized cerebral and cerebellar atrophy.

The clinical presentation remains fairly stable and may be associated with cerebellar atrophy.

We report an early-onset autosomal-recessive neurological disease with cerebellar atrophy and lysosomal dysfunction.

The diagnosis was made because of marked cerebellar atrophy in the repeated MRI.

Magnetic resonance imaging of the brains of our patients revealed marked cerebellar atrophy.

Successive magnetic resonance imaging (MRI) revealed progressive cerebellar atrophy, explaining the ataxia.

Histology revealed inner ear hair cell loss and cerebellar atrophy.

Pathologically, brain MRIs also suggest variability, with prominent cortical as well as cerebellar atrophy.

Brain MRI scans showed diffuse hypomyelination associated with cerebellar atrophy.

MRI brain showed cerebellar atrophy with diffuse white matter hyperintensities.

In some cases, optic neuropathies are associated with cerebellar atrophy which mainly affects the vermis.

These findings provide support for the hypothesis that cerebellar atrophy in epilepsy affects procedural memory.

Here, we describe a Moroccan girl of consanguineous parents with optic atrophy and cerebellar atrophy.

Perturbations of protein folding and organelle crosstalk have been implicated in neurodegenerative processes including cerebellar atrophy.

The cerebellar atrophy predominantly affected the anterior lobe.

There were different degrees of cortical and cerebellar atrophy on brain MRI, but no hippocampal changes.