Skip to main content
. 2013 Oct;34(10):2034–2038. doi: 10.3174/ajnr.A3560

Fig 1.

Fig 1.

Type 1. Nonspecific brain atrophy. T1WI (A) and T2WI (B) of a 9-year-old patient (case 4) with an ATRX mutation of the ADD domain in exon 6 (c.390_391 ins A; E131fs). Nonprogressive diffuse cortical brain atrophy and ventricular enlargement due to loss of white matter volume are shown.