Stargardt Disease (Juvenile Macular Degeneration)
General: Onset between ages 8 and 14 years; variable appearance in different familie 424f58e s.
Ocular: Heredomacular dystrophy; bilateral lesions showing some degree of symmetry; chorioretinal heredodegeneration; abnormal color vision.
Clinical: Possible association with neurologic deficits, including spastic tetraparesis and cerebellar involvement.
Cibis GV, et al. Dominantly inherited macular dystrophy with flecks (Stargardt). Arch Ophthalmol 1980; 98: 1785-l789.
Hadden OB, Gass JDM. Fundus flavimaculatus and Stargardt's disease. Am J Ophthalmol 1976; 82:527.
Kalfakis N, et al. Stargardt's disease with neurological involvement: case report. Funct Neurol 1994; 9:97-l00.
Mantyjarvi M, Tuppurainen K. Color vision in Stargardt's disease. Int Ophthalmol 1992; 16:423-428.
Moloney JBM, et al. Retinal function in Stargardt's disease and fundus flavimaculatus. Am J Ophthalmol 1983; 96:57-65.
Noble KG, Carr RE. Stargardt's diseases and fundus flavimaculatus. Arch Ophthalmol 1979; 97:1281-l285.
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