Is there a cure for retinitis pigmentosa or nightblindness?

No. Retinitis pigmentosa (rp) is a defect in the lining tissue under the retina called the retinal pigment epithelium (rpe). It can be hereditary or sporadic , affect males or females, be found alone or with hearing or other neurological abnormalities. Treatment options are still experimental involving stem cell implantation, or gene therapy but none of these treatments are available yet to the public.
Retinal Chip. Retinitis pigmentosa is a group of inherited disorders that cause degeneration of the retina and vision loss. Depending on the type, some vision can be retained throughout life, in other cases, not. The most common symptoms are night blindness and gradual loss of peripheral vision. There is a new retinal implant which restores crude central vision( argus ii) for those who are blind from rp.

Related Questions

Is there a cure for retinitis pigmentosa?

No. This is an inherited deficiency of support for the retinal light receptive cells. The result is a drop out of these cells and progressive loss of vision sometimes leaving a central island but sometimes little at all. A retinal specialist can help sort yours out if you have it. You can also estimate your fate by studying your family members if they have it. Read more...
Retinal Chip. Retinitis pigmentosa is a group of inherited disorders that cause degeneration of the retina. Depending on the type, some vision can be retained throughout life, in other cases, not. The most common symptoms are night blindness and gradual loss of peripheral vision. There is no cure, but there is a new retinal implant which restores crude central vision ( argus ii) for those who are blind from rp. Read more...

Could you explain what is retinitis pigmentosa?

Retinal degeneration. The retina lines the back of our eye and acts like the film of a camera. It "sees" the light. Retinitis pigmentosa (rp) is a group of diseases caused by defective genes that cause the retina to malfunction. It is most often inherited. Over time patients lose peripheral and then central vision from rp. There is no treatment but in some cases vitamins can slow its course. There is no cure. Read more...
Retinitis pigmentosa. Retinitis pigmentosa (rp) is a group of inherited disorders characterized by progressive peripheral vision loss and night vision difficulties that can eventually lead to central vision loss. Read more...

What is the significance of retinitis pigmentosa?

Considerable. Rp affects the victim most prominently as vision will be gradually diminished generally starting in the teen years and progressing through young adulthood. It also significantly affects those around such a person who may have to deal with a poorly sighted person. And society has a signficant burden of the support of such people. Read more...
Inherited Disease. Retinitis pigmentosa is a group of inherited disorders that cause degeneration of the retina and vision loss. The condition can be inherited in multiple ways and has a variety of symptoms. The most common ones are night blindness and gradual loss of peripheral vision. There is currently no proven medical treatment, however the argus ii retinal implant may be useful in end stage disease. Read more...

What are the odds of developing retinitis pigmentosa?

You would need to. have a parent who carries the gene for it to be expressed in you. If you don't have this problem in your family line, then it's rare that it would happen spontaneously. Read more...

What are the chances of randomly getting retinitis pigmentosa?

At birth / later? Rp is an inherited condition and occurs according to the laws of inheritance. The chances of getting it randomly (that is to say without any being in your ancestry) is low but is somewhere in the neighborhood of 1 in 4000. At age 34, if you have no symptoms you are almost certain not to get rp. Read more...
Inherited Disease. Retinitis pigmentosa is a group of inherited disorders that cause degeneration of the retina and vision loss. The condition can be inherited in multiple ways and rarely is caused by a new mutation. The most common symptoms are night blindness and gradual loss of peripheral vision. There is currently no proven medical treatment, however retinal implant( argus ii) may help in end-stage rp. Read more...

Is it possible for retinitis pigmentosa and colorblindness to be linked?

Yes. Some types of retinitis pigmentosa (rp) can be linked with a cone dystrophy so you have a bad combination of night blindness, visual field loss and decreased visual acuity and loss of color vision. Read more...
No link. These can occur concurrently and advanced retinitis pigmentosa always has a loss of color vision. Classical colorblindness is an inherited disease also, but carried on a different part of the chromosome and is inherited independently of the genes for retinitis pigmentosa. So both can occur together if one inherits both but they are not linked. Read more...