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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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DALL·E 2025-01-27 00.35.46 - A vibrant and uplifting digital illustration of children depi

BECAUSE THEY ARE RARE & BEAUTIFUL


Discover our SuperHeroes all around the world.
 

Discover their incredible strength, resilience, and inspiring stories from around the world.
 

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LMBRD2 Everywhere In The World

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LMBRD2 GENE MUTATION. FOR US TO PROVIDE FAMILIES WITH NEEDED


Support Families, Empower Lives.

LMBRD2 country
LMBRD2 city
LMBRD2 continent
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LMBRD2 street

Discover our LMBRD2 Online Store

Spreading Awareness Through Our LMBRD2 Store

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