Vitreous Degeneration in Myopia and Retinitis Pigmentosa

  • R. C. Pruett
  • D. M. Albert


Myopia is the most common ocular disorder diagnosed and managed by the ophthalmologist; retinitis pigmentosa (RP) is seen infrequently. Why consider them together? In many cases both can be shown to have a hereditary basis. This suggests a fundamental metabolic abnormality, that they are “molecular” diseases. Each presents a wide spectrum of severity. Advanced forms of both show decreased retinal function, and both are characterized by premature cataract formation and vitreous degeneration. In a review of similarities and differences, certain notions arise that suggest explanations for clinical observations and present questions for future research.


Retinal Pigment Epithelium Retinal Detachment Retinitis Pigmentosa Macular Hole Proliferative Diabetic Retinopathy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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© Springer Science+Business Media New York 1987

Authors and Affiliations

  • R. C. Pruett
  • D. M. Albert

There are no affiliations available

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