Lennox-Gastaut syndrome (LGS) is an epilepsy syndrome that can develop over time from childhood seizures that remain uncontrolled by treatments.
Plan to be a part of our 2020 virtual conference on Saturday May 30th 09:00am--01:00pm AEST. Registration is free and you can register via Eventbrite. Because of COVID-19, the meeting…
The global coronavirus pandemic has brought significant challenges for us all, but particularly for children with developmental and epileptic encephalopathies.
The global coronavirus pandemic has brought significant challenges particularly for those with children with developmental and epileptic encephalopathies.
Prof Ingrid Scheffer discusses COVID-19 and issues relevant to children and adults with genetic epilepsy / DEEs and their families.
Global Genes connects, empowers and inspires the rare disease community and fosters collaboration between groups from around the world.
Having a child with SCN2A can have a significant impact on the whole family. Three parents tell their stories about having a child with SCN2A.
Mutations of the SCN2A gene can result in a range of different clinical syndromes. Understanding these clinical presentations can help to guide treatment.
What are the needs of families when their children with genetic epilepsy become unwell? Kris Pierce discusses the outcome from a recent roundtable.
What is the relationship between loss of function SCN2A mutations and autism? What can SCN2A mutations teach us about mechanisms underpinning autism?