Decreased FA in females with FX, and increased fiber density in males with FX, have both been found in frontostriatal regions.119,120

Functional connectivity We were unable to find any studies of functional connectivity in Fragile X. 22q11.2 Deletion syndrome 22q11.2 Deletion syndrome (22q DS), also called velocardiofacial syndrome and DiGeorge syndrome (among other names), is caused by a deletion on chromosome 22 and results in a heterogeneous spectrum of physiological, neurological, and psychological Inhibitors,research,lifescience,medical symptoms.121 Several of the 30 genes encoded in the deleted segment are highly expressed in the developing brain and known to affect early neuronal migration. Several neuroimaging studies have pointed to abnormal Inhibitors,research,lifescience,medical patterns of cortical thinning and white matter impairments. Structural MRI In a cross-sectional

study, Schaer et al found altered developmental trajectories of cortical thickness in 22q DS, with a decreased rate of thinning in childhood followed by an increased rate of cortical thinning in late adolescence (Supplementary Figure 3).122 Supplementary Figure 3. Differences in cortical thickness in 22q11.2 DS. Using repeated-measures with the longitudinal subsample, they confirm the different trajectories Inhibitors,research,lifescience,medical of cortical thickness changes observed with cross-sectional design. 122 In preadolescents (before 9 of age … This study built on earlier work by Bearden et al suggesting Inhibitors,research,lifescience,medical regionally specific cortical thinning in 22q DS, in superior parietal cortices and right parie to-occipital cortex, regions critical for http://www.selleckchem.com/products/VX-770.html visuospatial processing, and bilaterally in the most inferior portion of the inferior frontal gyrus (pars orbitalis), a key area for language development.123 A later study of the same cohort also used fractal

dimension analysis to reveal altered complexity and gyrification in 22q DS,124 a further index of disturbed cortical development. Studies of volumetric changes in the gray matter in 22q DS have found reductions in the cerebellum Inhibitors,research,lifescience,medical and posterior areas of the posterior and occipital areas and expansions in the frontal lobes,125,126 although one group found reductions in the frontal lobe as well.127 Looking specifically at which isothipendyl individuals with 22q DS developed psychosis, Gothelf et al found that greater reduction of the left DLPFC predicted greater psychotic symptoms. 22q DS is a heterogeneous disorder, which predisposes individuals to a range of other psychiatric and neurological issues.128 This heterogeneity might explain some of the lack of agreement across studies. In the white matter, volume is reduced in individuals with 22q DS, across the cerebellum, internal capsule, and frontal cortex.125,126 Srivastava et al found abnormalities in the development of the cortical gyri in children with 22q DS, specifically in areas important for visuospatial, attentional, and numerical cognition tasks.