If you've just received a diagnosis involving LMBRD2 mutations, you're not alone. We're here to help.

Why Your Information Matters
LMBRD2-related conditions are extremely rare, with only a small number of families worldwide affected. As the global patient registry, we collect information from families to:

• Connect researchers with the data needed to understand this condition

• Identify patterns across different children that could improve care

• Support research funding by demonstrating the scope of LMBRD2 conditions

• Build a community of families who can support each other

 

Your family's experience is valuable. Every piece of information helps researchers make progress toward better treatments.

What Happens Next
When you contact us, we'll:

• Welcome you to our community

• Send you a comprehensive questionnaire about your child's condition

• Connect you with other families and the latest research updates

• Provide ongoing support and information

 

Ready to connect? You can email us or fill out the form below. We'll respond promptly and send you the detailed questionnaire.