By David L. LevensonPosted May 17, 2018 09:02:49An eye doctor and a research group at the University of Florida are studying whether a common condition known as retinal detachment can lead to blurred vision.
They have found that people who have the condition, known as oculogyne, have reduced amounts of retinal collagen in the retina and a loss of retinas pigment.
In a study published in the journal Current Biology, they compared retinal protein levels and retinal pigmentation in 30 people who had the condition to 30 people with normal vision.
The researchers found that patients with retinal pigment loss had higher levels of retinoid-producing proteins.
Retinal pigment is an important component of the retina that allows the visual system to tell the wearer’s eye from his or her own.
Retinal protein is essential to maintaining proper vision.
Retinoid levels are linked to vision.
Retinoids are found in the eye cream and the eyeshadow.
They are derived from the plant retinol, which is derived from red algae.
Scientists have known for decades that retinoids can be damaged by the elements in the environment, including ultraviolet rays, UVB radiation, and the effects of ultraviolet radiation from sunlight.
The study found that the retinogenic proteins could be damaged in the absence of the retinal proteins.
The retinogens, such as retinoplastin, and retinoblastin could also be damaged when the retinas cells are exposed to ultraviolet light.
However, they were not damaged in a clinical setting.
The new study adds to the body of research linking retinosis and retinoic acid deficiency to the disorder, which affects around 7 million Americans.
The condition can cause blurry vision and can lead people to miss hours of work or school.
People who have retinitis pigmentosa (RP), which is found in 20 percent of people, may also have a loss in retinal retinoma (RTV), which affects less than 2 percent of the population.RTV is the most common form of retinoidosis.
People with the disorder have damage to the retina of the optic nerve.
People with RP can also develop other problems including macular degeneration and progressive retinal atrophy.
The findings suggest that RP patients may not be the only ones with retinopathies, according to Dr. Susan L. Durbin, director of the Eye and Vision Center at the Florida Eye Institute at the university.
“We have been doing studies over the last decade that have shown retinopathy in people with RP and RP alone, but no studies have been done to see if there are also RP patients with RTV and RTV alone,” Durbini said.
“The reason for that is that there are no studies that have looked at those patients with RP alone.”
She said that the study is an example of the work that is still needed to understand why RP can cause retinotoxicity.
“Retinotoxic retinoids are a very challenging disease because it involves many different proteins, and you can have very different proteins in the same cell, and they interact very differently,” Durini said, referring to the different proteins that cause retinoinosis.
“It is difficult to understand how the different retinocins interact in the body, so that could be why we haven’t seen any clear pattern of interactions in the RTV group.”
Dr. Lili-Lynn Rader, an associate professor of ophthalmic surgery at the Mayo Clinic, who was not involved in the study, said that a study like this may be the first step to better understanding how retinoctin proteins interact in humans.
“This is the first study that really looks at how retinotic proteins interact with each other in the human body,” she said.
Rader noted that the RAVP group is small.
It is likely that they have more people with retinoatitis pigmentosum who have RP than people with RAV.
In addition to Durbine, the researchers include researchers from the University at Albany in New York, the University College of London, the National Eye Institute, the Mayo Foundation Center for Human Development, and UCLA.