All cases of cerebral palsy warrant genomic screening
- PMID: 34114233
- DOI: 10.1111/dmcn.14951
All cases of cerebral palsy warrant genomic screening
Comment on
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Genetic testing in individuals with cerebral palsy.Dev Med Child Neurol. 2021 Dec;63(12):1448-1455. doi: 10.1111/dmcn.14948. Epub 2021 Jun 10. Dev Med Child Neurol. 2021. PMID: 34114234 Free PMC article.
References
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- May HJ, Fasheun JA, Bain JM, et al. Genetic testing in people with cerebral palsy. Dev Med Child Neurol 2021; 63: 1448-55.
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- Moreno-De-Luca A, Millan F, Pesacreta DR, et al. Molecular diagnostic yield of exome sequencing in patients with cerebral palsy. JAMA 2021; 325: 467-75.
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- Jin SC, Lewis SA, Bakhtiari S, et al. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy. Nat Genet 2020; 52: 1046-56.
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- Sartwelle TP, Johnston JC. Cerebral palsy litigation: change course or abandon ship. J Child Neurol 2015; 30: 828-41.
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- MacLennan AH, Gecz J, Perez-Jurado L. A genomic cause of cerebral palsy should not change the clinical classification. Ann Clin Transl Neurol 2018; 5: 1011.
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