Retinal dystrophies are a heterogeneous group of diseases in which the retina degenerates, leading to either partial or complete blindness. The severe and clearly hereditary forms, retinitis ...

PYC Therapeutics advances VP-001 for retinitis pigmentosa, gaining FDA insights for its upcoming registrational trial.

In addition, three specific mutations of the rhodopsin ( RHO) gene, which typically causes autosomal dominant-retinitis pigmentosa (see section on rod-cone dystrophies), have been associated with ...

Lipoprotein(a) is thought to contribute to ASCVD through proinflammatory, prothrombotic, and/or other proatherogenic mechanisms. 3, 9 Current evidence suggests that lipoprotein(a) is causal in the ...