gyrate atrophies การใช้

• Thus, gyrate atrophy can be found with either disorder, with proline deficiency as an underlying feature.
• "' Ornithine aminotransferase deficiency "'( also known as "'gyrate atrophy of the choroid and retina "') is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase.
• Gyrate atrophy is an inherited degenerative disorder of the retina and choroid, sometimes accompanying the metabolic condition tissues, while processes behind hyperornithinemia disrupt the metabolic pathway from ornithine to proline, which alters the catabolism of ornithine, and also results in reduced levels of proline.