Retinal follow-up in retinitis pigmentosa

Retinitis Pigmentosa
Treatment

Genetic evaluation, retinal follow-up and rehabilitation to preserve current vision and monitor the progression of the disease.

About Retinitis Pigmentosa Treatment

In retinitis pigmentosa, the aim is to preserve current vision and monitor the progression of the disease. The approach is largely based on genetic evaluation, follow-up and rehabilitation.

Retinitis pigmentosa is a genetic disease characterised by the progressive loss of retinal cells; it first affects night vision and then peripheral vision. The course and pace vary from person to person according to the genetic type.

Genetic counselling and regular retinal examinations are important in managing the process; gene therapies and stem cell research are promising. For the symptoms, see our Retinitis Pigmentosa page.

Who Is It For and When Is It Used?

Management of retinitis pigmentosa is planned in the following situations:

  • Difficulty with night vision: In patients with vision loss in dim environments who need diagnosis and follow-up.
  • Narrowing of the visual field: Regular visual field follow-up in cases developing tunnel vision.
  • Family history: Genetic evaluation in people with similar complaints in their family.
  • Difficulty in daily life: In patients who may benefit from low vision rehabilitation.
  • Accompanying cataract: Treatment of accompanying conditions that further reduce vision.

Treatment Methods

The main approaches used in retinitis pigmentosa:

  • Genetic evaluation: Allows the hereditary nature of the disease to be examined and family members to be informed.
  • Retinal follow-up: Regular retinal examinations and visual field follow-up monitor the course of the disease.
  • Low vision rehabilitation: With magnifiers and special devices, can help improve patients’ quality of daily life.
  • Gene therapies and stem cell research: Promising research is ongoing today in certain gene types.

Featured Approaches

Follow-up & Support

Preserving Vision

Retinal examination icon

Regular follow-up and rehabilitation to preserve current vision and support quality of life.

1
Regular monitoring

Follow-up

The course is monitored with visual field and retinal follow-up.

2
Rehabilitation

Low Vision

Current vision is used efficiently with magnifiers and devices.

3
Accompanying issues

Management

Conditions such as cataract are treated appropriately.

Quality of Life Preserved

Genetics & Future

Counselling & Research

Genetic counselling icon

Genetic counselling and assessment of emerging treatments for suitable candidates.

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Genetic counselling

Counselling

The inheritance type is determined and the family informed.

2
Suitability

Candidate

Candidacy for gene therapy is assessed in certain gene types.

3
Developments

Research

Stem cell and implant studies are followed.

Promising Approaches

Do you have a family history?

A comprehensive assessment is planned for early diagnosis, follow-up and genetic counselling.

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Benefits & Follow-up

What Rehabilitation Offers

Low vision rehabilitation increases independence in daily life.

  • Magnifier and device support
  • Preserving daily living skills
  • Improved quality of life

Regular Follow-up

Regular retinal and visual field follow-up is important in managing the process.

  • Visual field follow-up
  • Management of accompanying diseases
  • Genetic counselling

Frequently Asked Questions

In most types there is no definitive cure yet; the approach is based on follow-up, preserving vision and rehabilitation. Developments such as gene therapy in certain gene types are promising.
Genetic evaluation determines the inheritance type, clarifies the risks for family members and shows whether suitable patients are candidates for emerging treatments.
With magnifiers, special devices and training, current vision is used as efficiently as possible, which increases independence in daily life.
The course is highly variable according to the genetic type. In many patients vision can be preserved for many years; regular follow-up is important to managing the process.
The disease is genetic and the risk of passing to children varies according to the inheritance pattern. Genetic counselling is recommended to clarify this risk.
In some cases supplements may come into play on the doctor’s advice; however, these are not definitive solutions that stop the disease and should be assessed under specialist supervision.