09/03/2026
๐๐ถ๐๐ถ๐ป๐ด ๐ต๐ผ๐ฝ๐ฒ ๐ฎ๐ป๐ฑ ๐๐ฟ๐ฎ๐ป๐๐ณ๐ผ๐ฟ๐บ๐ถ๐ป๐ด ๐น๐ถ๐๐ฒ๐ ๐ณ๐ผ๐ฟ ๐ณ๐ฎ๐บ๐ถ๐น๐ถ๐ฒ๐ ๐น๐ถ๐๐ถ๐ป๐ด ๐๐ถ๐๐ต ๐ฟ๐ฎ๐ฟ๐ฒ ๐ฑ๐ถ๐๐ฒ๐ฎ๐๐ฒ ๐งฌโค๏ธ
For families living with a rare disease, the diagnostic journey can be long and filled with uncertainty.
At KKH Rare Disease Day 2026, we celebrated something extraordinary โ the life changing impact of the ๐๐ฆ๐ฏ๐ฐ๐ฎ๐ช๐ค๐ด ๐ง๐ฐ๐ณ ๐๐ช๐ฅ๐ด ๐ช๐ฏ ๐๐๐๐๐ ๐ฑ๐ณ๐ฐ๐จ๐ณ๐ข๐ฎ๐ฎ๐ฆ. ๐โจ
Funded by Temasek Foundation, this regional programme has been redefining paediatric rare disease care:
๐น 510 families across Singapore, Malaysia, the Philippines, and Vietnam gained access to genomic sequencing.
๐น 52% received a definitive diagnosis โ surpassing international benchmarks.
๐น From 7 years to just weeks โ dramatically shortening the diagnostic journey.
And this is just the beginning.
The programme is establishing ASEANโs first dedicated genetic registry โ a powerful shared resource that will strengthen diagnostics and personalised treatments for the regionโs multi-ethnic populations.
To our ASEAN collaborators, and most of all, our patients and their families โ thank you for allowing us to turn uncertainty into answers, and answers into hope. ๐ค
๐ Read more about Genomics for Kids for ASEAN. Link in the comments.
A new genetic registry under the Genomics for Kids in ASEAN programme will deepen understanding of rare diseases in Southeast Asia. Read more at straitstimes.com. Read more at straitstimes.com.