From the case: Huntington disease

Axial T2
Modality: MRI (T2)

- “ Huntington disease (Huntington chorea), is an autosomal dominant neurodegenerative disease in which there is trinucleotide (CAG) repeat. It is cau...”

View full size version of Huntington disease

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.