Stargardt Disease, an inherited eye disease, is a form of retinal dystrophy that primarily affects the macula—the central region of the retina responsible for sharp vision.
Unlike age-related macular degeneration, which typically occurs later in life, Stargardt Disease often begins in childhood or adolescence due to mutations in the ABCA4 gene.
This condition leads to progressive vision loss, starting with central vision impairment, blind spots, and visual distortion. Over time, lipofuscin deposits accumulate in the retinal pigment epithelium (RPE), damaging both cone and rod photoreceptors.
While there is no cure yet, advancements in vision aids like Vision Buddy glasses for Stargardt Disease offer new hope for effectively managing this condition.
Stargardt Disease is often referred to as juvenile macular degeneration due to its early onset. It affects the macula, leading to a gradual decline in central vision due to damage to cone photoreceptors, essential for color and detailed vision.
Key features of Stargardt Disease include:
Yellow deposits (lipofuscin): Accumulation in the RPE, disrupting normal function.
Stargardt Disease, an inherited retinal dystrophy, results in a loss of visual acuity, making detailed tasks like reading or sewing difficult. Patients often develop blind spots in their central vision, complicating navigation and daily life activities.
Additionally, damage to cone photoreceptors impairs color vision, further affecting the quality of life.
Advanced imaging techniques like Optical Coherence Tomography (OCT) and fundus photography are crucial for identifying macular damage and tracking the disease’s progression. Here are some key points to understand:
Vision Buddy glasses offer a transformative solution for patients with Stargardt Disease:
Patients report significant improvements in tasks like:
Specifically engineered glasses for Stargardt Disease.
Key features include:
Unlike age-related macular degeneration, which typically occurs later in life, Stargardt Disease often begins in childhood or adolescence due to mutations in the ABCA4 gene.
This condition leads to progressive vision loss, starting with central vision impairment, blind spots, and visual distortion. Over time, lipofuscin deposits accumulate in the retinal pigment epithelium (RPE), damaging both cone and rod photoreceptors.
While there is no cure yet, advancements in vision aids like Vision Buddy glasses for Stargardt Disease offer new hope for effectively managing this condition.
Stargardt Disease, an inherited retinal dystrophy, results in a loss of visual acuity, making detailed tasks like reading or sewing difficult. Patients often develop blind spots in their central vision, complicating navigation and daily life activities.
Additionally, damage to cone photoreceptors impairs color vision, further affecting the quality of life.
Advanced imaging techniques like Optical Coherence Tomography (OCT) and fundus photography are crucial for identifying macular damage and tracking the disease’s progression. Here are some key points to understand:
Vision Buddy glasses offer a transformative solution for patients with Stargardt Disease:
Patients report significant improvements in tasks like:
Specifically engineered glasses for Stargardt Disease.
Don’t let Stargardt Disease limit your world. Explore the possibilities with Vision Buddy
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