BESTS DISEASE: A CASE REPORT

BESTS DISEASE: A CASE REPORT

Bests disease is an autosomal dominant hereditary macular dystrophy characterized by the presence of auto-fluorescent vitelline deposits. We report a case of a vitelliform stage of bests disease in a 23-year-old female patient. The diagnosis was made based on the fundus appearance: egg yolk macular...

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Veröffentlicht in:International journal of advanced research (Indore) 2022-12, Vol.10 (12), p.512-514
Hauptverfasser: Haddougui, Soukaina, Brarou, Houda, Bajjouk, Salma, Bouchaar, Mounia, Mouzari, Yassine, Oubaaz, Abdelbarre
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container_issue 12
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container_title International journal of advanced research (Indore)
container_volume 10
creator Haddougui, Soukaina
Brarou, Houda
Bajjouk, Salma
Bouchaar, Mounia
Mouzari, Yassine
Oubaaz, Abdelbarre
description Bests disease is an autosomal dominant hereditary macular dystrophy characterized by the presence of auto-fluorescent vitelline deposits. We report a case of a vitelliform stage of bests disease in a 23-year-old female patient. The diagnosis was made based on the fundus appearance: egg yolk macular lesion, hypofluorescence in the early stages, OCT appearance and alteration of the electro-oculogram and the electroretinogram. The exact frequency of this condition is difficult to determine and varies according to the various studies. It is thought to account for 4% of all retinal dystrophies. Its management is an annual surveillance.
doi_str_mv 10.21474/IJAR01/15867
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