The genetic basis of cerebral palsy.
Dev Med Child Neurol
; 59(5): 462-469, 2017 05.
Article
em En
| MEDLINE
| ID: mdl-28042670
Although prematurity and hypoxic-ischaemic injury are well-recognized contributors to the pathogenesis of cerebral palsy (CP), as many as one-third of children with CP may lack traditional risk factors. For many of these children, a genetic basis to their condition is suspected. Recent findings have implicated copy number variants and mutations in single genes in children with CP. Current studies are limited by relatively small patient numbers, the underlying genetic heterogeneity identified, and the paucity of validation studies that have been performed. However, several genes mapping to intersecting pathways controlling neurodevelopment and neuronal connectivity have been identified. Analogous to other neurodevelopmental disorders such as autism and intellectual disability, the genomic architecture of CP is likely to be highly complex. Although we are just beginning to understand genetic contributions to CP, new insights are anticipated to serve as a unique window into the neurobiology of CP and suggest new targets for intervention.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Paralisia Cerebral
/
Variações do Número de Cópias de DNA
/
Mutação
Tipo de estudo:
Etiology_studies
/
Prognostic_studies
/
Risk_factors_studies
Limite:
Humans
Idioma:
En
Revista:
Dev Med Child Neurol
Ano de publicação:
2017
Tipo de documento:
Article
País de afiliação:
Austrália