Fig. 1From: A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case reportBrain MRI of the patient with high signal intensity of the white matter in axial T2, the arrows show high signal in the corpus callosum (a), low signal intensity of the white matter in sagittal T1 (b), low signal in the splenium of corpus callosum (arrow B) and diffuse high signal intensity of the white matter in coronal Flair (arrows c)Back to article page