Alport syndrome is a group of inherited conditions ... hearing loss – is caused by mutations in the type IV collagen gene and defective glomerular basement membrane.

Alport syndrome is a genetic disorder associated with kidney dysfunction, sensorineural hearing loss, and ocular abnormalities. In the kidneys, hematuria occurs in the early stages of the disease ...

Researchers at University of Tsukuba developed a novel imaging method for visualizing lesions in the glomerular basement membrane using a mouse model of Alport syndrome, a hereditary kidney disease.

The knockout of Col4a3 in mice is used as a model of Alport syndrome. Knockout mice develop glomerular disease associated with neutral lipid accumulation in the kidney and progressive renal failure, ...

said Kenneth Greenberg, PhD, CEO of SonoThera, who will be presenting the Company’s session focused on nonviral gene therapy for X-linked Alport Syndrome.

THE Pride of St Helens Awards, sponsored by Mikhail Hotel & Leisure Group, will take place on Friday, November 22.

Data from Eloxx’s proof-of-concept trial in patients with nonsense mutation Alport Syndrome (NMAS) presented in late-breaking ...

said Kenneth Greenberg, PhD, CEO of SonoThera, who will be presenting the Company’s session focused on nonviral gene therapy for X-linked Alport Syndrome. Session Details: Title: Development of ...

Neurogene has reported encouraging efficacy results with its gene therapy for rare genetic disorder Rett syndrome, but investors' concerns about safety seem to be weighing on its share price.