Reviewed by Grant M. Comer, M.D., M.S.
On this page:
- What Is Retinoschisis?
- Risk Factors
- Tests and Diagnosis
- Treatment and Drugs
- Clinic Information
Retinoschisis is a condition in which an area of the retina (the tissue lining the inside of the back of the eye that transmits visual signals to the optic nerve and brain) has separated into two layers. The part of the retina that is affected by retinoschisis will have suboptimal vision. This can occur in different layers of the retina, and for different reasons.
The two major causes of retinoschisis are:
Juvenile X-linked Retinoschisis
Juvenile X-linked Retinoschisis is a genetic disease of the retina and affects primarily boys and young men. In this form of retinoschisis, a mutation or abnormal gene is carried on the X chromosome. Men have only one X chromosome, while women have two. Therefore, women can carry the condition, but because they almost always have another normal X chromosome, they typically retain normal vision, even as carriers. Men, on the other hand, will develop subnormal vision if they have an affected X chromosome.
This condition typically presents during childhood and is estimated to affect one in 5,000 to 25,000 individuals. Affected males are usually identified in grade school, but occasionally are identified as young infants. Affected boys and men should have periodic eye examinations.
Degenerative retinoschisis is the splitting of the retina as a result of aging. It can affect men and women. This is not a genetic condition.
Retinoschisis affects two primary aspects of vision.
- Central vision can be impaired, with visual acuity ranging from 20/30 to less than 20/200. Acuity loss is caused by the formation of tiny cysts between the separated layers of the retina. These cysts often form a "spoke-wheel" pattern which is very subtle and is usually detected only by a trained clinician. Since the nerve tissue is damaged by these cysts, visual acuity cannot be improved with glasses.
- Peripheral vision can also be lost if the inner layer of nerve cells split off from the outer layer of cells.
Retinoschisis can be confused with other eye diseases, such as amblyopia (lazy eye). If someone in your family has retinoschisis and you are diagnosed with amblyopia you should have a thorough exam by an ophthalmologist experienced in diagnosing this condition.
- Decreased central vision
- Decreased peripheral vision
The symptoms described above may not necessarily mean that you have retinoschisis. However, if you experience one or more of these symptoms, contact your eye doctor for a complete exam.
The two major causes of retinoschisis are:
- Genetic (typically occurring in younger patients)
- Degenerative (typically occurring in older patients)
Retinal detachment can occur if the anchoring of the outer layer of the retina to the eye wall is impaired. Since retinoschisis patients are more susceptible to retinal detachment, they should have regular examinations with an ophthalmologist. When detected early, a complicating retinal detachment can be treated surgically; however, splitting or schisis of the retina itself cannot be corrected by medication or surgery.
The electroretinogram (ERG) is used to assess function of the nerve tissue in the retina. The eye is stimulated with light after either dark or light adaptation. Contact lenses, embedded with an electrode to measure electrical impulses created by the functioning retina, are worn by the patient. The reaction of the eye to various light stimuli is recorded and evaluated. This test documents the type of photoreceptor activity and the overall function of the inner and outer layers of the retina, and is a very important tool in diagnosis.
ERGs are easily obtained on adults and children under 24 months of age. However, ERGs performed on children between the ages of two and five can be difficult and often require general anesthesia. Therefore, we encourage the testing be done before age two or after age five. In general, after age five, nearly all children can have an ERG without any difficulties.
Beginning at age 3-4, all children, even without retinoschisis, should have their vision checked yearly and glasses prescribed as necessary. Children who show schisis of the peripheral retina need more frequent examinations. We feel these examinations should be conducted by a subspecialty trained retina surgeon, since surgery would be required if a retinal detachment were to develop. Follow-up intervals are best determined by the doctor who is following your child.
Currently, there are no medical or surgical treatments available for retinoschisis.
Glasses may improve the overall quality of vision in a patient with retinoschisis who is also near-sighted or farsighted, but will not "repair" the nerve tissue damage from the retinoschisis.
Vitamin A does not appear to help in retinoschisis. Vitamin A may have benefits for other genetic retinal diseases, particularly in cases of retinitis pigmentosa where the retinal nerve cells are slowly dying. However, retinoschisis is quite different from retinitis pigmentosa, since the retinal cells and their connections in retinoschisis are mechanically disrupted but are not thought to be dying.