![]() These mutations were estimated to contributed to death in 9% of cases. The researchers identified 11 particular mutations that were likely to cause health problems. In such cases, the mutation also showed up in the offspring 80% of the time-again, more often than would be expected by chance. A handful of potentially harmful mutations in these genes occurred in parents. Most were “de novo” mutations, meaning that while they were found in the child, they weren’t found in either parent. They found that in SUDC cases, these genes contained significantly more mutations than would be expected by chance. The researchers then focused on 137 genes associated with heart or seizure disorders, both of which can trigger sudden death. ![]() There weren’t enough subjects to uncover genetic associations in a broad, initial analysis. The team first sequenced whole exomes, the 1% of the human genome that codes for proteins. Results appeared in Proceedings of the National Academy of Sciences on December 28, 2021. NIH’s National Institute on Drug Abuse (NIDA) and National Institute of Mental Health (NIMH) supported the work. ![]() DNA was extracted from samples collected through the SUDC Registry and Research Collaborative. To do so, they sequenced DNA from 124 SUDC cases and their parents. Richard Tsien and Orrin Devinsky at the NYU Grossman School of Medicine sought to identify genetic mutations that might contribute to SUDC. While SIDS cases outnumber SUDC cases by four to one, research funding and published studies for SIDS have dwarfed that for SUDC.Ī research team led by Drs. In children 1 year of age or older, it’s called sudden unexplained death in children (SUDC). When it happens in children under 1 year of age, it's called sudden infant death syndrome (SIDS). Ann in the uk / ShutterstockĪpproximately 1,800 children in the United States die from sudden, unexplained causes each year, most while asleep. ![]() Researchers have been working to understand the causes of sudden unexplained death in children. ![]()
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