[角膜格子状营养不良的临床考量与遗传学]
[Clinical considerations and genetics of the lattice dystrophy of the cornea].
作者信息
Hammerstein W, Scholz W
出版信息
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1975;193(2):109-20. doi: 10.1007/BF00419355.
PMID:164138
Abstract
Lattice dystrophy of the cornea is reported in 4 families. For purposes of linkage analysis we did serological tests on pertinent family members, including marker testing of the blood group systems ABO, MNSs, Rh, K, Ky, and P; protein group systems Hp, Ge, Gm, and Inv; and enzyme polymorphisms SEP, PGM, ADA, and AK.
摘要
在4个家族中报告了角膜格子状营养不良。为了进行连锁分析，我们对相关家庭成员进行了血清学检测，包括血型系统ABO、MNSs、Rh、K、Ky和P的标记检测；蛋白组系统Hp、Ge、Gm和Inv；以及酶多态性SEP、PGM、ADA和AK。
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