Farmer S G, Longstreth W T, Kalina R E, Todorov A B
Am J Ophthalmol. 1985 Jan 15;99(1):45-50. doi: 10.1016/s0002-9394(14)75865-9.
We examined members of two families with Kjellin's syndrome, an autosomal recessive disorder characterized by spastic paraparesis, dementia, and macular changes. Although the retinal lesions resemble the flecks of fundus flavimaculatus by ophthalmoscopy, they appear distinct from previously reported retinal flecks by fluorescein angiography.
我们研究了两个患有凯尔林综合征的家族成员，这是一种常染色体隐性疾病，其特征为痉挛性截瘫、痴呆和黄斑病变。尽管通过检眼镜检查发现视网膜病变类似于黄斑营养不良的眼底斑点，但通过荧光素血管造影显示，它们与先前报道的视网膜斑点明显不同。
