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Ciitizen is partnering with the SCN2A community and rare disease groups to empower patients and families with access to their health data and advance research.

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SCN2A Asia PacificFollow

Working towards a cure for SCN2A, Raising Awareness and SCN2A Organisation for SCN2A families in Australia & across South East Asia.

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pedneurojournal @pedneurojournal·

6 Jan

Does genetic testing change #epilepsy treatment?

Genetic cause in 25% infant/ped onset epilepsy
- Impact treatment in 45%:
- 36% antiseizure med choice
- 7% vitamin/metabolic tx
- 3% pathway-driven off-label use med
- 10% gene-specific clinical trials
https://bit.ly/3VTqJ10

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SCN2A Asia Pacific @SCN2AAustralia·

22 Dec

In 2022, SCN2A Asia Pacific has been able to increase our impact due to the support of our partners and sponsors.

We would like to thank @epilepsy_fdn for their support of our mission and for helping us with our activities in 2022. #SCN2A

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SCN2A Asia Pacific @SCN2AAustralia·

22 Dec

In 2022, SCN2A Asia Pacific has been able to increase our impact due to the support of our partners and sponsors.

We would like to thank @OxPharmaGenesis for their support of our mission and for helping us with our activities in 2022. #SCN2A

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