There is renewed hope for treatment of a rare genetic condition, Progeria, that causes rapidly accelerated aging and leads to an average life expectancy of 13 years.
Scientists studying the genes of two infants who died of mysterious illnesses found the infants had mutations in LMNA, the same gene altered in patients with the premature aging condition. But the infants' unusual mutations caused them to make many more bad copies of the gene's primary protein, lamin A, than progeria patients.