Brain Asymmetry Mapped in Velo-vardio-facial Syndrome and in Normally Developing Children
نویسندگان
چکیده
Introduction: Differences in structure and function between the two brain hemispheres have generated great interest in neuroscience, revealing the developmental origins of lateralized cognitive functions and hemispheric specialization of neuronal circuitry [4]. Anatomical asymmetries develop in utero and increase during childhood, so any derailment in the course of neurodevelopment may lead to an abnormal pattern of asymmetry. Here we performed the first tensor-based morphometry (TBM) study of brain asymmetry, to our knowledge. We examined patterns of structural brain asymmetries in a sample of children with 22q11.2 deletion syndrome (22q11.2DS; also known as velo-cardio-facial syndrome: VCFS), and in a well-matched sample of normally developing children. Abnormal brain asymmetry is reported in at least some patients with 22q11.2DS, which is also thought to predispose individuals to the development of schizophrenia.
منابع مشابه
Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2).
BACKGROUND This study evaluated differences in caudate volumes in subjects with velo-cardio-facial syndrome due to a 22q11.2 (22qDS) deletion. Because psychosis is observed in 30% of adult subjects with 22qDS, this neurogenetic disorder could represent a putative model for a genetically mediated subtype of schizophrenia. METHODS Caudate volumes were measured on high-resolution magnetic resona...
متن کامل22q11.2 Deletion Syndrome
In 1965 DiGeorge described a patient with hypoparathyroidism and cellular immune deficiency secondary to thymic hypoplasia. Soon the pattern of malformation included in this syndrome expanded to include other defects of third and fourth branchial arches as well as dysmorphic facial features. In 1978 Shprintzen reported a group of children with cleft palate or velopharyngeal incompetence, cardia...
متن کامل22q11.2 Deletion Syndrome
In 1965 DiGeorge described a patient with hypoparathyroidism and cellular immune deficiency secondary to thymic hypoplasia. Soon the pattern of malformation included in this syndrome expanded to include other defects of third and fourth branchial arches as well as dysmorphic facial features. In 1978 Shprintzen reported a group of children with cleft palate or velopharyngeal incompetence, cardia...
متن کامل22q11.2 Deletion Syndrome
In 1965 DiGeorge described a patient with hypoparathyroidism and cellular immune deficiency secondary to thymic hypoplasia. Soon the pattern of malformation included in this syndrome expanded to include other defects of third and fourth branchial arches as well as dysmorphic facial features. In 1978 Shprintzen reported a group of children with cleft palate or velopharyngeal incompetence, cardia...
متن کامل22q11.2 Deletion Syndrome
In 1965 DiGeorge described a patient with hypoparathyroidism and cellular immune deficiency secondary to thymic hypoplasia. Soon the pattern of malformation included in this syndrome expanded to include other defects of third and fourth branchial arches as well as dysmorphic facial features. In 1978 Shprintzen reported a group of children with cleft palate or velopharyngeal incompetence, cardia...
متن کامل