Genetic testing in cerebral palsy with clinical and neuroimaging variables
Genetic testing has a role in determining CP aetiology; however, there is no consensus on who should be tested. We used mixed methodology and found that dysmorphic features, intellectual disability, and 'MRI not compatible with the clinical picture' are most supportive of a genetic cause of CP.
Authors
- Simon Paget (ORCID: https://orcid.org/0000-0001-6605-3330)
- Esther Tantsis (ORCID: https://orcid.org/0000-0003-3414-3889)
- Michael Fahey (ORCID: https://orcid.org/0000-0003-0811-4785)
- Michelle A. Farrar (ORCID: https://orcid.org/0000-0002-4472-0902)
- Dianah Abd Hadi
- Connor R. Goldman
- Russell C. Dale (ORCID: https://orcid.org/0000-0002-2495-1826)
- Velda X. Han (ORCID: https://orcid.org/0000-0003-4633-4316)
- Shekeeb S. Mohammad (ORCID: https://orcid.org/0000-0003-1219-4781)
- Yisselle I. Virella‐Perez
Institutions
- The University of Sydney (AU)
- Hospital Kuala Lumpur (MY)
- Children's Hospital at Westmead (AU)
- UNSW Sydney (AU)
- Monash Children’s Hospital (AU)
- The Centers (US)
- Sydney Children’s Hospitals Network (AU)
- National University Health System (SG)
- Monash University (AU)
Publication Details
- Journal
- Developmental Medicine & Child Neurology
- Published
- 2025-04-05
- DOI
- https://doi.org/10.1111/dmcn.16323
- Citations
- 3
- Primary Topic
- Cerebral Palsy and Movement Disorders
- Type
- article
- Field-Weighted Citation Impact
- 4.41
Funders
- Cerebral Palsy Alliance