PRIMARY MESODERMAL DYSGENESIS OF THE CORNEA (PETERS ANOMALY) IN 2 BROTHERS

被引：14

作者：

BOEL, M

TIMMERMANS, J

EMMERY, L

DRALANDS, G

FRYNS, JP

VANDENBERGHE, H

机构：

[1] DEPT HUMAN BIOL,DIV HUMAN GENET,MINDERBROEDERSSTR 12,B-3000 LEUVEN,BELGIUM

[2] CATHOLIC UNIV LEUVEN,DEPT OPHTHALMOL,B-3000 LOUVAIN,BELGIUM

来源：

HUMAN GENETICS | 1979年 / 51卷 / 02期

关键词：

D O I：

10.1007/BF00287184

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

In this report two brothers with a severe form of Peters' anomaly, i.e., primary dysgenesis mesodermalis of the cornea, are described. The thirddegree consanguinity of the parents is an additional argument for the autosomal recessive inheritance of this condition. © 1979 Springer-Verlag.

引用

页码：237 / 240

页数：4

共 9 条

[1]

Alkemade P., 1969, DYSGENESIS MESODERMA

[2] A NEW OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION [J].