Multimodal imaging of a patient with RAB39B mutation.

Abstract excerpt

Mutations in RAB39B gene have been linked to intellectual deficiency associated with parkinsonism, also referred as to Waisman syndrome. As it appears to be a very rare cause of Parkinson Disease (PD), with only few cases described in the literature, the typical clinical and radiological features are yet to be determined. In this article, we report and illustrate multimodal brain imaging by computed tomography,...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Positron-Emission Tomography
• Share to Fluorodeoxyglucose F18
• Share to Multimodal Imaging