On this sequence ...
Sagittal T1
On this sequence we can see some thinning of the corpus callosum with cerebellar atrophy.
Modality: MRI (T1)

- “ This patient was homozygous for the most common mutation in NPC, I1061T. Whilst this case is normally associated with juvenile onset and death bef...”

View full size version of Niemann-Pick disease: type C

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