Fig. 1From: A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndromePlain head and abdominal computed tomography (CT) scans of the proband. a, b. Head CT. Severe calcification was observed in the basal ganglia, thalamus, deep white matter (a), and cerebellum (b) (arrow). c. Abdominal CT. Renal dysplasia can be seen on the right side (arrow)Back to article page