Fig. 2From: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genesBrain MR investigation of index-patient (III.1, pictures a, b, c) and her mother (II.1, pictures d, e, f). Hypoplasia of the corpus callosum is revealed in both patients (red arrows). Otherwise no other structural anomalies were observedBack to article page