Stargardt Disease

A genetic disease that blocks the body from properly removing waste. This usually leads to lipofuscin buildup on the macula, leading to vision loss.

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Treatments

Currently, there is currently no cure for Stargardt disease. However, ongoing research is exploring potential treatments and interventions. Management typically involves low-vision aids and devices to assist individuals in their daily activities. Genetic counseling is also an important aspect for families with a history of Stargardt disease, as it helps individuals understand the inheritance pattern and make informed decisions.

It's important to note that developments in medical research and treatments may have occurred since my last update. If you or someone you know is affected by Stargardt disease, it is recommended to consult with an eye care professional or a genetic counselor for the latest information and guidance.

Gene Therapy

A process that uses viruses to replace faulty genes in retinal cells with healthy ones in order to stop or slow vision loss from inherited diseases.

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Normal vision vs. Stargardt Disease

Overview

Stargardt disease, also known as Stargardt macular dystrophy or juvenile macular degeneration, is a genetic eye disorder that affects the macula, a small, specialized area in the center of the retina responsible for sharp, central vision. Stargardt disease is typically diagnosed in children and young adults and is one of the most common forms of inherited juvenile macular degeneration.

Key Characteristics

Macular Degeneration

Stargardt disease leads to the progressive degeneration of the cells in the macula, resulting in a gradual loss of central vision.

Inheritance

Stargardt disease is usually inherited in an autosomal recessive manner, meaning that a person must inherit a mutated gene from both parents to develop the condition. The specific gene associated with Stargardt disease is the ABCA4 gene.

Onset

Symptoms often appear in childhood or adolescence, and individuals may notice a gradual decline in central vision. However, the age of onset and the rate of progression can vary.

Treatments

Currently, there is currently no cure for Stargardt disease. However, ongoing research is exploring potential treatments and interventions. Management typically involves low-vision aids and devices to assist individuals in their daily activities. Genetic counseling is also an important aspect for families with a history of Stargardt disease, as it helps individuals understand the inheritance pattern and make informed decisions.

It's important to note that developments in medical research and treatments may have occurred since my last update. If you or someone you know is affected by Stargardt disease, it is recommended to consult with an eye care professional or a genetic counselor for the latest information and guidance.

Overview

Stargardt disease, also known as Stargardt macular dystrophy or juvenile macular degeneration, is a genetic eye disorder that affects the macula, a small, specialized area in the center of the retina responsible for sharp, central vision. Stargardt disease is typically diagnosed in children and young adults and is one of the most common forms of inherited juvenile macular degeneration.

Key Characteristics

Macular Degeneration

Stargardt disease leads to the progressive degeneration of the cells in the macula, resulting in a gradual loss of central vision.

Inheritance

Stargardt disease is usually inherited in an autosomal recessive manner, meaning that a person must inherit a mutated gene from both parents to develop the condition. The specific gene associated with Stargardt disease is the ABCA4 gene.

Onset

Symptoms often appear in childhood or adolescence, and individuals may notice a gradual decline in central vision. However, the age of onset and the rate of progression can vary.

Treatments

Currently, there is currently no cure for Stargardt disease. However, ongoing research is exploring potential treatments and interventions. Management typically involves low-vision aids and devices to assist individuals in their daily activities. Genetic counseling is also an important aspect for families with a history of Stargardt disease, as it helps individuals understand the inheritance pattern and make informed decisions.

It's important to note that developments in medical research and treatments may have occurred since my last update. If you or someone you know is affected by Stargardt disease, it is recommended to consult with an eye care professional or a genetic counselor for the latest information and guidance.

Overview

Stargardt disease, also known as Stargardt macular dystrophy or juvenile macular degeneration, is a genetic eye disorder that affects the macula, a small, specialized area in the center of the retina responsible for sharp, central vision. Stargardt disease is typically diagnosed in children and young adults and is one of the most common forms of inherited juvenile macular degeneration.

Key Characteristics

Macular Degeneration

Stargardt disease leads to the progressive degeneration of the cells in the macula, resulting in a gradual loss of central vision.

Inheritance

Stargardt disease is usually inherited in an autosomal recessive manner, meaning that a person must inherit a mutated gene from both parents to develop the condition. The specific gene associated with Stargardt disease is the ABCA4 gene.

Onset

Symptoms often appear in childhood or adolescence, and individuals may notice a gradual decline in central vision. However, the age of onset and the rate of progression can vary.

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