The CdLS Foundation: A Legacy of Support
The CdLS Foundation has a rich history of supporting families and research initiatives related to CdLS. Their commitment to fostering scientific advancements and providing resources to those affected by CdLS is integral to our mission. By sponsoring our research, you are partnering with a foundation deeply rooted in making a meaningful difference in the CdLS community.
Advancing Understanding of SMC3 Mutations in CdLS
Cornelia de Lange Syndrome (CdLS) presents diverse challenges, with mutations like SMC3 being less understood. Recognizing this, we've established a dedicated team of researchers focusing on SMC3, particularly the mutation affecting Vihaan. This team brings together experts in genetics,
Your Contributions: Directly Supporting Targeted Research
Every donation received is earmarked specifically for SMC3-CdLS research. Your support enables this focused team to delve deeper into understanding and potentially treating this rare mutation.