Background: PRKAG2 syndrome is an inherited disease caused by mutations in the PRKAG2 gene, which encodes the γ2 regulatory subunit of AMP-activated protein kinase (AMPK). These mutations result in ...
Noah was diagnosed with a rare birth defect, called Wolff-Parkinson-White syndrome, a condition his family had no idea he had. "A lot of the arrythmia disorders like Wolff-Parkinson-White ...
Nov. 12, 2024 — Researchers have identified a potential biomarker of Parkinson's disease progression. According to the new study, patients with a slow progression of ... Oct. 8, 2024 ...
At the screening, the electrocardiogram was abnormal. A pediatric cardiologist diagnosed Hudson had Wolff-Parkinson-White syndrome, which is caused when an extra electrical pathway in the heart ...
He previously had been diagnosed in high school with Wolff-Parkinson-White syndrome, another heart issue. “I always believed in myself, and my family helped with that so much, just always ...