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Whole genome sequencing in cerebral palsy: a UK paediatric pilot study

30 Jul 2026

Abstract excerpt

Background: Prior international studies indicate that 9-36% of people with cerebral palsy (CP) have a monogenic condition. However, the utility of whole genome sequencing (WGS) as a diagnostic tool for United Kingdom (UK) National Health Service (NHS) patients has not been evaluated. Methods: This prospective pilot study recruited 86 individuals with CP from specialist clinics in Bedford, Cambridge, Colchester,...

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Share to Cerebral Palsy and Movement Disorders
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PMID: 42571358
DOI: 10.1016/j.lanepe.2026.101786

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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