Test tubes and bad equipment in a research lab

Upcoming webinar explores genetics and CP 

Cerebral Palsy Alliance is excited to share an upcoming webinar that will explore the groundbreaking potential of the understanding and treating of neurological conditions, including cerebral palsy through genome sequencing.

Cerebral palsy, the leading cause of childhood disability globally, has long been linked to birth-related complications. Yet, recent research indicates that genetic factors may play a more significant role than previously understood. 

This webinar, run by Genomics England, draws on the latest research to explore the important role of genomics in providing answers and hope for those living with cerebral palsy. 

Participants will hear from experts on the importance of family engagement in genetic testing and the ethical considerations involved. Additionally, a parent of a child with cerebral palsy who has received a genetic diagnosis will share their personal journey and advocacy efforts. 

Event Details 

The free event will be recorded and sent to those who registered who cannot make the time of this UK webinar.  

Date & Time: 

Friday, 11 October 2024 1:00 AM, (Sydney time) 

Thursday, 10 October 2024, 16:00 PM (London time) 

Registration: https://www.genomicsengland.co.uk/events/neurological-conditions-webinar

Rare conditions impact over 350 million people worldwide, and nearly half of these conditions present neurologically. For many, getting a genetic diagnosis is still difficult, especially for rare childhood neurological conditions. 

However, advancements in whole genome sequencing are uncovering the genetic causes behind some of these conditions, opening up new discussions and options for diagnosis and treatment. 

Cerebral Palsy Alliance Research Foundation (CPARF) is funding another research study being carried out by this group, and while this research is not being presented in the webinar, preliminary findings are showing promising results. The study revealed that 33% of cerebral palsy cases in the study had a genomic link, as presented by UK-based PhD student Tracy Lau at the 2024 European Society of Human Genetics meeting.  

Register for this informative session to learn more about how genomics is helping us understand neurological conditions and how it is bringing hope to families and shaping the future of treatment for cerebral palsy and other related disabilities. 

Register here: https://www.genomicsengland.co.uk/events/neurological-conditions-webinar