Kjellin Syndrome
General: Autosomal recessive disorder; degeneration progressive.
Ocular: Yellow retinal flecks that lie at the pigment epithelial level; poor visual perceptual skills; central retinal degeneration.
Clinical: Spastic paraparesis; dementia; progressive lower extremity weakness; dysarthric speech; muscle atrophy.
Farmer SG, et al. Fleck retina in Kjellin's syndrome. Am J Ophthalmol 1985; 99:45-50.
Kjellin K. Familial spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration. Arch Neurol 1959; 1: 133.
Traboulsi EI. Fleck retina in Kjellin's syndrome. Am J Ophthalmol 1985; 99:738-739.
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