Juvenile Macular Dystrophy (JMD) is sometimes referred to as Juvenile Macular Degeneration. It is different from age-related macular degeneration (AMD). AMD occurs as part of natural aging. Normal aging processes can lead to structural and blood flow changes that can predispose patients to AMD.
Juvenile macular degeneration is a rare, genetic condition that affects vision early in life. JMD causes central vision loss and often begins in childhood into young adulthood.
The most common forms of JMD are:
• Stargardts Disease
• Best's Disease
• Juvenile Retinoschisis
Unfortunately, there is no treatment. However, there are several treatments under clinical trials to manage these diseases, which may help to slow the progression and preserve vision longer
Visual aids, adaptive training, and other tools can help with vision loss.
JMD damages the macula, the tissue in the center of the retina at the back of the eye. This area provides sharp central vision.
All forms of JMD cause problems with central vision. Some children do not show signs of having JMD. A healthcare professional may identify an issue during a comprehensive eye exam.
A doctor may use family history to determine a child's risk, as well as special labs, which may be used to conduct genetic testing that can help to identify the exact gene that is linked to the disease.
The eye doctor may also proceed with other tests to confirm or rule out JMD diseases, those tests may include:
• OCT
• Fluorescein Angiography
• ERG (Electroretinography)
Source:
• www.aao.org
• www.webmd.com
• www.medicalnewstoday.com
• www.pmc.ncbi.nlm.nih.go
Photo Source:
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www.opticalimages.com
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