Skip to main content
Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Exome sequencing in paediatric patients with movement disorders

Fig. 2

Brain Magnetic Resonance Imaging (MRI) of 2 patients with variants identified in SPG11. a Brain MRI of Patient 19 and 30 with periventricular white matter changes; b brain MRI of Patient 19 and 30 with thinning of corpus callosum. Arrows indicated the area with periventricular white matter changes and thinning of corpus callosum

Back to article page