Bietti's crystalline dystrophy
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| Bietti's crystalline dystrophy Classification and external resources | |
| OMIM | 210370 |
|---|---|
| DiseasesDB | 33427 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Phone:617-525-6884
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Overview
Bietti's crystalline dystrophy (BCD), also called Bietti's crystalline retinopathy, is a rare autosomal recessive eye disease named for Dr. G. B. Bietti.[1]
BCD is a rare disease and appears to be more common in people with Asian ancestry.
Presentation
The symptoms of BCD include: crystals in the cornea (the clear covering of the eye); yellow, shiny deposits on the retina; and progressive atrophy of the retina, choriocapillaries and choroid (the back layers of the eye). This tends to lead to progressive night blindness and visual field constriction.
Genetics
It has been associated with CYP4V2.[1]
References
External links
- Bietti's Crystalline Dystrophy Resource Guide from the National Eye Institute (NEI).
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Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
