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  • Epilepsies Action Network

Undiagnosed Disease Network Funded at $18M for FY23

Epilepsies Action Network alongside other thought leaders for The Epilepsies advocated to the Senate and House Appropriations Committees for $10M in funding for the Undiagnosed Disease Network (UDN).


We are thrilled to report $18M was awarded! We are happy to be part of the broad advocates sharing the import of this program in identifying and understanding some of the most difficult to diagnose and rare medical conditions.


As of Dec 2022, the UDN had evaluated 2020 medical cases. They identified a diagnosis in 607 many of which had epilepsy as a symptom.


Genetic variants associated with seizures identified by UDN included: CDK19, WDR37, TIAM1, ROBO1, FZR1, RNF2, CAPZA2, EIF2AKI, OXR1, CACNA1A, ATAD2A and DNMIL.


Epilepsy Action Network proudly acknowledges our partners and co-signors including:


Child Neurology Foundation (CNF)

CURE Epilepsy

Danny Did Foundation

Decoding Developmental Epilepsies

DEE-P Connections

Epilepsy Alliance America

Epilepsy Foundation (National)

Epilepsy Learning Healthcare System

Global Genes

The Inchstone Project

Pediatric Epilepsy Research Consortium (PERC)

Rare Epilepsy Network (REN)



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