Understanding Okur-Chung Neurodevelopmental Syndrome

Help us fund research into Okur-Chung Neurodevelopmental Syndrome (OCNDS), a rare genetic disorder affecting children’s neurological development. Your donation supports scientific research to better understand the condition and develop treatments, while also providing essential resources
and support for affected families.

Read more abour this syndrome :https://www.csnk2a1foundation.org/

Aidez-nous à financer la recherche sur le syndrome neurodéveloppemental d'Okur-Chung (OCNDS),une maladie génétique rare qui affecte le développement neurologique des enfants. Votre don soutient la recherche scientifique pour mieux comprendre cette maladie et développer des traitements, tout en fournissant des ressources essentielles et un accompagnement aux familles concernées.

En savoir plus sur ce syndrome :https://www.csnk2a1foundation.org/
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Why donate?

The Foundation For Rare Diseases is a foundation for scientific cooperation which aims at accelerating research for all rare diseases.
Your generosity allows us to act concretely to help the 30 000 million people concerned in Europe. 
The Foudnation For Rare Diseases's mission are to :
  • identify the cause of rare diseases and accelerate diagnosis,
  • support the development of treatments,
  • improve patient's and faamilies everyday life.

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