
ALONE WE GO FASTER
BUT TOGETHER
WE GO FURTHER
Welcome to the LMBRD2 community! We understand that facing a rare genetic disorder can feel isolating, but you are not alone. Here, families and supporters come together to provide hope, strength, and resources for those affected by LMBRD2 gene mutation. Whether you’re newly diagnosed or looking to support our cause, we stand united in this fight.

30
Children Since 2021
1
Medical Publication in 2021
3%
Of Births With Genetic Disorder
We Are A Non-Profit Association
We Are A World Wide Organization
 
Our association connects families, researchers, and medical professionals worldwide to raise awareness of LMBRD2 gene mutation related genetic disorders. We aim to support affected individuals and their families, fund research, and advocate for improved diagnostics, treatments, and care. Together, we strive to advance understanding and create a stronger, more hopeful future for those impacted by this rare condition.
LMBRD2 Gene Mutation - Recent News & Updates
Spreading Awareness Through News & Updates

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