家族性IIa型高脂蛋白血症伴结晶状角膜营养不良（施奈德型）（作者译）
[Crystalline corneal dystrophy (Schnyder) in the presence of familial type IIa hyperlipoproteinaemia (author's transl)].
作者信息
Thiel H J, Voigt G J, Parwaresch M R
出版信息
Klin Monbl Augenheilkd. 1977 Nov;171(5):678-84.
PMID:202777
Abstract
A family with dominant autosomal hyperlipoproteinaemia typ IIa is reported. One sibling, a 19-year-old man, showed in addition to the hyperlipoproteinaemia typical corneal signs of crystalline corneal dystrophy of Schnyder. From 1964 to 1976 these corneal deposits increased. The problems of hyperlipoproteinaemia combined with corneal crystalline dystrophy are discussed.
摘要
报告了一个患有显性常染色体IIa型高脂蛋白血症的家族。一名19岁男性同胞除了患有高脂蛋白血症外，还表现出典型的施奈德结晶性角膜营养不良的角膜体征。从1964年到1976年，这些角膜沉积物有所增加。讨论了高脂蛋白血症合并角膜结晶性营养不良的问题。
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