3q29 microdeletion syndrome is a recurrent subtelomeric deletion syndrome with variable clinical manifestations including intellectual deficit and dysmorphic features.
Comprehensive, easy-to-understand information about this condition
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The 3q29 Foundation was created by families, advocates, and researchers of this rare genetic syndrome. With a Board of Directors, Scientific Advisory Board, and Advisory Group, they're a committed team of volunteers ready to remove the obscurity from this genetic syndrome.
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.