Alpers-Huttenlocher syndrome (AHS) is a rare autosomal recessive disease caused by a mutation in the POLG1 gene.AHS primarily impacts the brain and liver, leading to various symptoms, with seizures and liver failure.
Our platform aims to expedite research and development for children with rare diseases by integrating stem cell research with advanced molecular biology and tissue engineering.
Join us in making a difference! Volunteer and help support Stemnovate's groundbreaking research to find cures for rare childhood diseases.