Full 2L QBank
Ophthalmology General 1b80901d

A young patient presents to the ophthalmology clinic with loss of central vision. There is no obvious family history. ERG and EOG were observed to be normal. Which of the following is the most likely diagnosis?

A
Stargardt's disease
B
Best's Vitelliform Dystrophy
C
Retinitis Pigmentosa
D
Cone- Rod Dystrophy
High-Yield Explanation
Loss of central vision with a normal ERG and EOG is consistent with a diagnosis of Stargardt's disease. Stargardt's disease is an autosomal recessive disorder and hence a negative family history is not uncommon.

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