Central nervous system (CNS) dysfunction is a cardinal feature in 22q11 deletion. The underlying CNS abnormalities remain, however, unknown. We report unilateral hemispheric polymicrogyria in a child with 22q11 deletion presenting with hemiplegia and cognitive and behavioural disorders. This observation widens the spectrum of brain malformations associated with this genetic defect. It further suggests a relationship between the 22q11 deletion and disorders of cerebral gyration. It would therefore be interesting to look for neuronal migration disorders in patients with 22q11 deletion presenting neurological signs, and on the other hand to screen for 22q11 deletion in patients with isolated neuronal migration disorders
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...
Chromosome 22q11.2 deletion syndrome (22q11.2DS), a neurogenetic condition, is the most common micro...
Polymicrogyria (PMG) is a brain malformation due to abnormal cortical organisation. It is a heteroge...
Several brain malformations have been described in rare patients with the deletion 22q11.2 syndrome ...
Background and purposeMR imaging studies and neuropathologic findings in individuals with 22q11.2 de...
Movement abnormalities are frequently reported in children with 22q11.2 deletion syndrome (22q11.2DS...
Movement abnormalities are frequently reported in children with 22q11.2 deletion syndrome (22q11.2DS...
Evidence is rapidly accumulating that rare, recurrent copy number variants represent large effect ri...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22. 2...
Abstract22q11.2 deletion syndrome (22q11DS) is the most common pathogenic copy number variant in hum...
22q11 Deletion syndrome (22q11DS) is a neurogenetic disorder, resulting from a hemizygous microdelet...
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...
Chromosome 22q11.2 deletion syndrome (22q11.2DS), a neurogenetic condition, is the most common micro...
Polymicrogyria (PMG) is a brain malformation due to abnormal cortical organisation. It is a heteroge...
Several brain malformations have been described in rare patients with the deletion 22q11.2 syndrome ...
Background and purposeMR imaging studies and neuropathologic findings in individuals with 22q11.2 de...
Movement abnormalities are frequently reported in children with 22q11.2 deletion syndrome (22q11.2DS...
Movement abnormalities are frequently reported in children with 22q11.2 deletion syndrome (22q11.2DS...
Evidence is rapidly accumulating that rare, recurrent copy number variants represent large effect ri...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22. 2...
Abstract22q11.2 deletion syndrome (22q11DS) is the most common pathogenic copy number variant in hum...
22q11 Deletion syndrome (22q11DS) is a neurogenetic disorder, resulting from a hemizygous microdelet...
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...
Chromosome 22q11.2 deletion syndrome (22q11.2DS), a neurogenetic condition, is the most common micro...