Scientists at UT Southwestern Medical Center have traced a rare premature aging condition in a young Malaysian man to a ...

“[...] this study addresses a critical gap by providing new insights into the role of telomere attrition across different progeroid conditions.” “[…] this ...

Researchers have defined a new genetic disease caused by a mutation in the IVNS1ABP gene. The condition marks a rare ...

“In sum, we have defined what a premature aging disease is and developed tools to allow diagnostics of patients and disease population.” “In this study, we have utilized phenome explorations to define ...

New research from Florida State University is beginning to piece together the stubborn puzzle posed by a family of rare and debilitating premature aging disorders. Most of these diseases, called ...

BALTIMORE, MD – A newly identified genetic disorder causing rapid aging has been named Garg-Mishra Progeroid Syndrome (GMPGS) in honor of its discoverers, Dr. Abhimanyu Garg and Dr. Prashant Mishra.

Sentynl will acquire full rights to the investigational drug candidate, Progerinin (SLC-D011), adding to its commercial ...

GREENVILLE, N.C. (WNCT) — Deallaney Hudson is a recent graduate from East Carolina University. She was born with a rare, genetic disease called Neonatal Progeroid Syndrome, which accelerates her aging ...

Deallaney Hudson has faced uncertainty since her birth and diagnosis of neonatal progeroid syndrome, a rare disorder characterized by accelerated aging. As she prepared for East Carolina University’s ...