Podcast
Lennox-Gastaut Syndrome
Lennox-Gastaut syndrome (LGS) is an epilepsy syndrome that can develop over time from childhood seizures that remain uncontrolled by treatments.
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Resources
Categories
Podcast
Supporting Children in Uncertain Times
The global coronavirus pandemic has brought significant challenges for us all, but particularly for children with developmental and epileptic encephalopathies.
Podcast
Strategies for Carers in Uncertain Times
The global coronavirus pandemic has brought significant challenges particularly for those with children with developmental and epileptic encephalopathies.
Podcast
COVID-19
Prof Ingrid Scheffer discusses COVID-19 and issues relevant to children and adults with genetic epilepsy / DEEs and their families.
Podcast
Global Genes
Global Genes connects, empowers and inspires the rare disease community and fosters collaboration between groups from around the world.
Podcast
Family Stories
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.
Webinar
Clinical Features of SCN2A-Related Disorders
Mutations of the SCN2A gene can result in a range of different clinical syndromes. Understanding these clinical presentations can help to guide treatment.
Podcast
Exploring Families’ Needs
What are the needs of families when their children with genetic epilepsy become unwell? Kris Pierce discusses the outcome from a recent roundtable.
Podcast
Loss of Function & Autism
What is the relationship between loss of function SCN2A mutations and autism? What can SCN2A mutations teach us about mechanisms underpinning autism?
Podcast
Models in Rare Diseases
Why are models needed to assess and develop treatments in rare diseases? What types of models are there? When are different models used?