
SARS-CoV-2 altered mitochondrial DNA methylation in Indian COVID-19 patients
I was reading an unrelated article about a boy who was developing normally in the ‘Medical Mysteries‘ section of the Wa Po titled - “A toddler’s wobbly walk, hand tremors send parents on a medical journey“ and long story short it identified a genetic issue induced by bad flu he had 15ish years ago as a toddler. It affected his mitochondria.
“At first, Wangler said, he was skeptical. Like other clinicians, he’d seen several patients with DNM1L mutations, but he said their physical symptoms — such as early-onset epilepsy — were different, and more severe, than Oliver’s.“What changed my mind was finding other families who have similar symptoms with the same identical gene variant,” Wangler said.The DNM1L gene provides instructions for making a crucial protein that helps mitochondria, the tiny powerhouses that supply energy to cells, divide and maintain their shape, Wangler said. DNM1L performs a similar role in peroxisomes, small cellular structures that help process specific fats and protect cells from oxidative damage, he added.”
So I searched for if DNM1L had been related to long covid and found this recent article and thought I’d pass it along immediately. Has anyone researched this?