KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity.
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| Title: | KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity. |
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| Authors: | Jadhav T; Department of Neurology, The Royal Children's Hospital, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia., Bouffler SE; Australian Genomics, Melbourne, Victoria, Australia., Innes E; Kids Neuroscience Centre, Children's Hospital at Westmead, Sydney, New South Wales, Australia., Fahey M; Department of Pediatric Neurology, Monash Health, Melbourne, Victoria, Australia.; Department of Pediatrics, Monash University, Melbourne, Victoria, Australia., Hunter M; Department of Pediatrics, Monash University, Melbourne, Victoria, Australia.; Monash Genetics, Monash Health, Melbourne, Victoria, Australia.; Genetic Counselling Liaison Service, Queensland Children's Hospital, Brisbane, Queensland, Australia., Kothur K; Kids Neuroscience Centre, Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia., Lunke S; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia., Lynch M; Neurosciences Unit, Queensland Children's Hospital, Brisbane, Queensland, Australia., Macdonald-Laurs E; Department of Neurology, The Royal Children's Hospital, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia., Palmer EE; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.; UNSW Medicine and Health, The University of New South Wales, Sydney, New South Wales, Australia., Patel C; Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia., Pinner J; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.; UNSW Medicine and Health, The University of New South Wales, Sydney, New South Wales, Australia., Riney K; Neurosciences Unit, Queensland Children's Hospital, Brisbane, Queensland, Australia.; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia., Sachdev R; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.; UNSW Medicine and Health, The University of New South Wales, Sydney, New South Wales, Australia., Sandaradura SA; Kids Neuroscience Centre, Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia., Scheffer IE; Department of Neurology, The Royal Children's Hospital, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia.; Department of Medicine, University of Melbourne, Austin Health, Melbourne, Victoria, Australia.; Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia., Stark Z; Australian Genomics, Melbourne, Victoria, Australia.; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia., Howell KB; Department of Neurology, The Royal Children's Hospital, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Pediatrics, The University of Melbourne, Melbourne, Victoria, Australia. |
| Source: | Epilepsia open [Epilepsia Open] 2026 Jun; Vol. 11 (3), pp. 949-961. Date of Electronic Publication: 2026 May 04. |
| Publication Type: | Journal Article; Multicenter Study |
| Journal Info: | Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101692036 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2470-9239 (Electronic) Linking ISSN: 24709239 NLM ISO Abbreviation: Epilepsia Open Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2470-9239 |
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| DOI: | 10.1002/epi4.70266 |
