Best Vitelliform Macular Dystrophy
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Best Vitelliform Macular Dystrophy is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Best macular dystrophy
- macular degeneration, polymorphic vitelline
- vitelliform macular dystrophy, early-onset
- vitelliform macular dystrophy, juvenile-onset
- vitelliform macular dystrophy, type 2
Best vitelliform macular dystrophy is an autosomal dominant genetic form of macular degeneration that usually begins in childhood or adolescence and slowly progresses to affect central vision. The age of onset and severity of vision loss are highly variable. Best vitelliform macular dystrophy is associated with an abnormality in the VMD2 gene.
American Council of the Blind
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American Foundation for the Blind
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Association for Macular Diseases, Inc.
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Foundation Fighting Blindness
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Genetic and Rare Diseases (GARD) Information Center
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NIH/National Eye Institute
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National Association for Parents of Children with Visual Impairments (NAPVI)
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This is an abstract of a report from the National Organization for Rare Disorders (NORD). A copy of the complete report can be downloaded free from the NORD website for registered users. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational therapies (if available), and references from medical literature. For a full-text version of this topic, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
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It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email firstname.lastname@example.org
Last Updated: 12/24/1969
Copyright 2007 National Organization for Rare Disorders, Inc.
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