Primary Hyperoxaluria Type 1 (PH1) is a rare genetic metabolic disorder that can lead to serious health issues, including ...

diPrimary hyperoxaluria type 1 (PH1 ... confirmed through a 24-hour urine analysis and genetic testing. Signs and symptoms generally vary from one person to another, but early detection is ...

The condition typically manifests in childhood with symptoms such as kidney stones ... "Success for YolTech’s hyperoxaluria ...

Beyond hyperoxaluria, Novome’s platform has potential ... peptides or nanobodies to alleviate symptoms, while avoiding systemic immune suppression. Beyond the gut, there is also growing evidence ...