Plasminogen Replacement Therapy for Congenital Plasminogen Deficiency

January 4, 2018

At Prometic Life Sciences we are committed to addressing unmet medical needs in rare diseases such as Congenital Plasminogen Deficiency (PLGD). Congenital PLGD is an inherited disorder passed on from generation to generation in which a person is born with two mutated genes, one from each parent. This is commonly referred to as an autosomal recessive pattern. It is caused by changes in the gene that gives instructions to make plasminogen (PLG).

For more information on PLGD, visit http://plasminogen.com/ 

Previous Video
Rare Disease: Alström Syndrome
Rare Disease: Alström Syndrome

Alström syndrome is a rare inherited autosomal recessive syndrome characterized by the onset of obesity in ...

Next Video
Prometic Life Sciences 2016 Update
Prometic Life Sciences 2016 Update

Prometic Life Sciences CEO Pierre Laurin gives an end of year update for 2016.