Vitelliform macular dystrophy

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD's medical weight loss NYC, sleep center NYC
Philadelphia medical weight loss and Philadelphia sleep clinics

Vitelliform macular dystrophy
File:Autosomal dominant - en.svg
Synonyms	Best disease, Best vitelliform macular dystrophy
Pronounce	N/A
Specialty	N/A
Symptoms	Vision loss, blurry vision, metamorphopsia
Complications	N/A
Onset	Childhood or early adulthood
Duration	Progressive
Types	N/A
Causes	Genetic mutations in the BEST1 gene
Risks	Family history of the condition
Diagnosis	Ophthalmoscopy, electrooculography, genetic testing
Differential diagnosis	Age-related macular degeneration, Stargardt disease
Prevention	N/A
Treatment	No cure, low vision aids, vitamin A supplementation
Medication	N/A
Prognosis	Variable, can lead to significant vision loss
Frequency	Rare
Deaths	N/A

Vitelliform macular dystrophy (VMD), also known as Best disease, is a rare, genetic eye disorder that affects the retina. It is characterized by the accumulation of yellowish material in the macula, the central part of the retina responsible for sharp, central vision.

Symptoms

The symptoms of Vitelliform macular dystrophy typically begin in childhood or adolescence, although they can appear later in life. The most common symptom is a gradual decline in central vision, which can affect one or both eyes. Other symptoms may include distorted vision (metamorphopsia), trouble distinguishing between colors (color blindness), and sensitivity to bright light (photophobia).

Causes

Vitelliform macular dystrophy is caused by mutations in the BEST1 gene. This gene provides instructions for making a protein that is found in the retina. The protein plays a crucial role in the normal functioning of the retina's light-sensing cells. Mutations in the BEST1 gene disrupt the normal functioning of these cells, leading to the symptoms of Vitelliform macular dystrophy.

Diagnosis

Diagnosis of Vitelliform macular dystrophy is typically made through a comprehensive eye examination, including a detailed examination of the retina. Additional tests may include electroretinography (ERG), optical coherence tomography (OCT), and genetic testing to identify mutations in the BEST1 gene.

Treatment

There is currently no cure for Vitelliform macular dystrophy. Treatment is focused on managing symptoms and slowing the progression of the disease. This may include the use of low-vision aids, such as magnifying glasses and large-print materials, and referral to services for individuals with visual impairment.

Prognosis

The prognosis for individuals with Vitelliform macular dystrophy varies. Some individuals may maintain good vision into adulthood, while others may experience a significant decline in vision. Regular follow-up with an ophthalmologist is important to monitor for changes in vision and to manage any complications that may arise.

See also

• Macular degeneration
• Retinal diseases
• Genetic disorders

References

   This article is a  stub. You can help WikiMD by expanding it!

This article is a stub related to genetics. You can help WikiMD by expanding it!