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Morsy, H.* ; Kim, H.* ; Jang, G.* ; Zaki, M.S.* ; Severino, M.* ; Abdelrazek, I.M.* ; Hussien, H.* ; Self, E.* ; Albaradie, R.S.* ; Bakur, K.* ; Firoozfar, Z.* ; Efthymiou, S.* ; Noureldeen, M.M.* ; Nabil, A.* ; Alvi, J.R.* ; Molavi, F.* ; Alavi, S.* ; Alibakhshi, R.* ; Topcu, V.* ; Mancilar, H.* ; Uctepe, E.* ; Yesilyurt, A.* ; Aldhalaan, H.* ; Showki Tous, E.S.* ; Alhaddad, B.* ; Elbendary, H.M.* ; Scardamaglia, A.* ; Murphy, D.* ; Yépez, V.A.* ; Gagneur, J. ; Omar, T.I.* ; Abd Elmaksoud, M.* ; Vandrovocova, J.* ; Abdalla, E.* ; Reilly, M.M.* ; Sultan, T.* ; Alkuraya, F.S.* ; Gleeson, J.G.* ; Um, J.W.* ; Houlden, H.* ; Ko, J.* ; Maarofian, R.*

MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy.

Am. J. Hum. Genet. 113, 380-391 (2026)
Verlagsversion Forschungsdaten DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
MDGA2 encodes a membrane-associated protein that is critical for regulating glutamatergic synapse development, modulating neuroligins (Nlgns), and maintaining excitatory-inhibitory synaptic balance. While MDGA2 functions have been extensively studied in murine and cellular models, its association with human developmental disorders has yet to be established. Through exome sequencing, we identified seven distinct homozygous loss-of-function variants in MDGA2 in nine individuals from seven consanguineous families, all presenting with developmental and epileptic encephalopathy (DEE). Clinically, these individuals exhibited a consistent phenotype including infantile hypotonia, severe neurodevelopmental delay, intractable seizures, along with distinct dysmorphic features. Neuroimaging findings included delayed/incomplete myelination, early-onset brain atrophy, white-matter thinning, basal ganglia volume loss, and small hippocampi. Functional studies of three representative nonsense variants revealed impaired MDGA2 membrane trafficking, disrupted Nlgn1 interaction, and perturbed MDGA2-mediated excitatory synaptic functions in mammalian expression systems and cultured hippocampal neurons. Our findings support the involvement of MDGA2 in a subtype of autosomal-recessive DEE. This not only underscores a loss-of-function pathogenic mechanism but also highlights the previously unrecognized role of MDGA2 in human synaptic development and regulation, significantly expanding our understanding of the genetic architecture of DEEs.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Mdga2 ; Epileptic Encephalopathy ; Excitatory Synapse ; Excitatory-inhibitory Balance ; Neurodevelopmental Disorder ; Neuroligin ; Synaptic Suppression
ISSN (print) / ISBN 0002-9297
e-ISSN 1537-6605
Zeitschrift American Journal of Human Genetics, The
Quellenangaben Band: 113, Heft: 2, Seiten: 380-391 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort New York, NY
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Computational Biology (ICB)
Förderungen Nile of Hope Hospital for Congenital Anomalies, Alexandria, Egypt
Wellcome Trust
UCL Global Engagement Fund scheme
National Research Foundation of Korea (NRF) - Ministry of Science and ICT
NRF - Ministry of Science and ICT
GERF-STDF
MRC
MSA Trust
National Institute for Health Research University College London Hospitals Biomedical Research Centre (NIHR-BRC)
FARA
Michael J. Fox Foundation (MJFF)
EAN
Fidelity Trust
Victoria Brain Bank
Rosetrees Trust
NIH NeuroBioBank
Dolby Family Fund
Queen Square BrainBank
Alzheimer's Research UK (ARUK)
MRC Brainbank Network
MSA Coalition
Deutsche Forschungsgemeinschaft (DFG
Parkinson Disease Society
European Union
Parkinson's Foundation
DFG
Guarantors of Brain
Cerebral Palsy Alliance