Adult foveomacular vitelliform dystrophy

Balarin, Valdir; Lira, Rodrigo Pessoa Cavalcanti; Berezowsky, Michel; Torigoe, Andréa Mara Simões

doi:10.1590/s0034-72802013000300013

Rev. bras.oftalmol.

2013

DOI: 10.1590/s0034-72802013000300013

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Adult foveomacular vitelliform dystrophy

Valdir Balarin

Rodrigo Pessoa Cavalcanti Lira

Michel Berezowsky

et al.

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2018

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“…Adult foveomacular vitelliform dystrophy is usually presents bilaterally but unilateral has also been seen, as well as bilateral form after unilateral onset. 5 Is a clinically heterogenous and pleomorphic disease, in which ophthalmoscopically changes often do not correspond with the visual function 3. AFVD may be visually asymptomatic or mild visual blurring and metamorphopsia in one or both eyes.…”

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confidence: 99%

Adult-onset vitelliform macular dystrophy: case report

Aragão¹,

Barreira²,

Carneiro³

et al. 2018

Rev. Med. UFC

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Adult-onset foveomacular vitelliform dystrophy is a rare disease. It shares heritance features with Best disease. Its onset is in the 3rd and 5th decade, and it is characterized by subretinal deposition of yellowish material in the foveal area. Visual acuity ranges from 20/25 to 20/50, which can be seen in routine examination. Patient remains with good visual function throughout theirs lives. Typically the electro-oculogram may be normal or subnormal. We present a case of adult-onset vitelliform macular dystrophy, diagnosed in a patient with complaint of bilateral blurred vision.

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mentioning

confidence: 99%

Adult-onset vitelliform macular dystrophy: case report

Aragão¹,

Barreira²,

Carneiro³

et al. 2018

Rev. Med. UFC

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Adult foveomacular vitelliform dystrophy

Cited by 1 publication

References 6 publications

Adult-onset vitelliform macular dystrophy: case report

Adult-onset vitelliform macular dystrophy: case report

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