Watch as Isabelle from the U.S. and her elementary school classmates learn about how the kidneys and liver work
and Isabelle shares what it’s like to live with PH1.
Primary hyperoxaluria type 1 (PH1) is a rare inherited disease of the liver in which overproduction of oxalate results in deposition of calcium oxalate crystals in the kidneys and urinary tract and can lead to the formation of recurrent kidney stones, progressive decline in kidney function, and multiorgan damage, when the disease advances.
Click here to learn more about PH1.
PH1 of a Kind is being developed by Alnylam Pharmaceuticals in partnership with the Oxalosis & Hyperoxaluria Foundation. To learn more about each organization and their work with PH1, click on the logos below.
*The characters featured in PH1 of a Kind are fictional. Any resemblance to actual people is purely coincidental.