|
|
Case three: Stargardt's disease (Fundus Flavimaculatus) or Juvenile Macular Degeneration |
|
|
|
Comments |
|
Stargardt's Disease (Fundus Flavimaculatus) or Juvenile Macular Degeneration, is thought to be an autosomal recessive disorder. Visual loss often begins in the first or second decade of life. A beaten bronze metal appearance in the central macula and yellow peripheral flecks along with a "dark" or "silent" choroid on fluorescein angiography are the hallmarks of this disease. Our patient, a 38 year old male, was referred for evaluation of decreased visual acuity of 1 to 1-1/2 years duration. On examination his VA was 20/50 OD and 20/200 OS. Family history was significant for a brother, age 40, who had decreased vision since age 10 which had been described as Juvenile macular degeneration. | |
[Return To:] |
|
Photo credit: , Director of Photography/Webmaster- Southeastern Eye Center |
|
[Home][Physicians][Subspecialties][Cataracts][Cataract FAQ] |