Reposted by Amy Wyler
New insights into Noonan syndrome with multiple lentigines reveal how specific genetic mutations drive heart muscle thickening and suggest dasatinib as a potential therapeutic approach. doi.org/g93vpk
Uncovering drivers of—and possible treatment for—Noonan syndrome heart defects
Noonan syndrome with multiple lentigines (NSML) is a rare genetic disorder that causes short stature, distinctive facial features, and clusters of dark skin spots called lentigines.
medicalxpress.com
September 16, 2025 at 6:47 PM
New insights into Noonan syndrome with multiple lentigines reveal how specific genetic mutations drive heart muscle thickening and suggest dasatinib as a potential therapeutic approach. doi.org/g93vpk