| Literature DB >> 27612489 |
Hannah C Kinney1, Annapurna H Poduri2, Jane B Cryan2, Robin L Haynes2, Lisa Teot2, Lynn A Sleeper2, Ingrid A Holm2, Gerald T Berry2, Sanjay P Prabhu2, Simon K Warfield2, Catherine Brownstein2, Harry S Abram2, Michael Kruer2, Walter L Kemp2, Beata Hargitai2, Joanne Gastrang2, Othon J Mena2, Elisabeth A Haas2, Roya Dastjerdi2, Dawna D Armstrong2, Richard D Goldstein2.
Abstract
Sudden infant death syndrome (SIDS) and sudden unexplained death in childhood (SUDC) are defined as sudden death in a child remaining unexplained despite autopsy and death scene investigation. They are distinguished from each other by age criteria, i.e. with SIDS under 1 year and SUDC over 1 year. Our separate studies of SIDS and SUDC provide evidence of shared hippocampal abnormalities, specifically focal dentate bilamination, a lesion classically associated with temporal lobe epilepsy, across the 2 groups. In this study, we characterized the clinicopathologic features in a retrospective case series of 32 children with sudden death and hippocampal formation (HF) maldevelopment. The greatest frequency of deaths was between 3 weeks and 3 years (81%, 26/32). Dentate anomalies were found across the pediatric age spectrum, supporting a common vulnerability that defies the 1-year age cutoff between SIDS and SUDC. Twelve cases (38%) had seizures, including 7 only with febrile seizures. Subicular anomalies were found in cases over 1 year of age and were associated with increased risk of febrile seizures. Sudden death associated with HF maldevelopment reflects a complex interaction of intrinsic and extrinsic factors that lead to death at different pediatric ages, and may be analogous to sudden unexplained death in epilepsy.Entities:
Keywords: Dentate gyrus; Febrile seizures; Granule cell dispersion; Sudden infant death syndrome (SIDS); Sudden unexpected death in pediatrics with hippocampal formation maldevelopment (SUDP-HFM); Sudden unexplained death in childhood (SUDC); Sudden unexplained death in epilepsy (SUDEP)
Year: 2016 PMID: 27612489 PMCID: PMC6281079 DOI: 10.1093/jnen/nlw075
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685