Choroidal dystrophies
The cornea allows light to enter the eye. As light passes through the eye the iris changes shape by expanding and letting more light through or constricting and letting less light through to change pupil size. The lens then changes shape to allow the accurate focusing of light on the retina. Light excites photoreceptors that eventually, through a chemical process, transmit nerve signals through the optic nerve to the brain. The brain processes these nerve impulses into sight.
- Electroretinography
- Fluorescein angiography
- Genetic testing
Definition
Choroidal dystrophy is an eye disorder involving the choroid, a layer of blood vessels between the sclera and retina.
Causes, incidence, and risk factors
Choroidal dystrophies are usually due to an abnormal gene (hereditary). It usually affects males, starting in childhood.
Symptoms
The first symptoms are peripheral vision loss and vision loss at night.
Signs and tests
An eye surgeon who specializes in the back of the eye (retina specialist) diagnoses choroidal dystrophies. The following tests may be needed to diagnose the condition:
Treatment
Choroidal dystrophies are usually treated with observation.
References
Grover S, Fishman GA. Choroidal dystrophies. In: Yanoff M, Duker JS, eds. Ophthalmology. 3rd ed. St. Louis, Mo: Mosby Elsevier; 2008:chap 6.
- Review date:
- October 27, 2009
- Reviewed by:
- Linda J. Vorvick, MD, Medical Director, MEDEX Northwest Division of Physician Assistant Studies, University of Washington, School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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