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Clinically Relevant Genes Identified in Cerebral Palsy Cohorts Following Evaluation of the Clinical Description and Phenotype: A Systematic ReviewA growing number of genes have been identified in individuals with cerebral palsy; however, many of these studies have poor compliance with the cerebral palsy clinical description. This systematic review aimed to assess the quality of the cerebral palsy clinical description/phenotype in cerebral palsy genetic studies published between 2010 and 2024 and report clinically relevant genes based on the quality of the cerebral palsy phenotype.
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Prenatal factors in cerebral palsyThis article discusses the prenatal factors associated with the development of infants born with cerebral palsy.
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Heavy maternal alcohol consumption and cerebral palsy in the offspringThe aim of this study was to investigate the association between heavy maternal alcohol consumption and pre- peri- and postneonatally acquired cerebral palsy.
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Obstetric malpractice litigation and cerebral palsy in term infantsThe aim of this paper is to review relevant research papers to aid practitioners involved in obstetric malpractice litigation.
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Migraine and preterm birthMaternal migraine, as self-reported early in pregnancy, was associated with preterm birth in survivors without CP & in infants who died in the perinatal period
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Cerebral PalsyA non-progressive motor disability due to damage of the developing brain, this is the most common physical disability in childhood. Affecting about one in 500 babies, it is frequently accompanied by other neurological impairments, such as intellectual or sensory.