January 26, 2019 - SCN2A Australia

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Welcome to SCN2A Australia

Happy Australia Day! Today we launch SCN2A Australia. We look forward to working with families, researchers, clinicians and professional bodies to improve the lives of

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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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SynGAP Research Fund (SRF)@cureSYNGAP1·

16 Mar

Kudos to @IDreamofGenes for this tremendous work covering 6 genes.

SYNGAP1
STXBP1
KCNQ2
FOXG1
SCN2A
SCN8A

Computation of longitudinal phenotypes in 466 individuals with a developmental and epileptic encephalopathy enables clinical trial readiness

https://www.medrxiv.org/content/10.1101/2023.03.02.23286645v1

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SWAN Australia @swanaus·

14 Mar

Over 150 SWAN children experience neurological symptoms as a result of their genetic condition. Some conditions include: Rubinstein-Taybi Syndrome, FOXP1 Syndrome, SCN2A, CACNA1A and a range of rare deletions and duplications.

#brainawarenessweek #neurological #SWANAus

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SCN2A Asia Pacific @SCN2AAustralia·

11 Mar

We are proud to partner with @geneticepilepsy to host this family day. Connection is so important in rare disease.

We can’t wait to meet you all!

#scn2a #family #raredisease @MelbourneZoo

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