两兄弟患有原发性角膜中胚层发育异常（彼得斯异常）。
Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers.
作者信息
Boel M, Timmermans J, Emmery L, Dralands G, Fryns J P, Van den Berghe H
出版信息
Hum Genet. 1979 Oct 1;51(2):237-40. doi: 10.1007/BF00287184.
PMID:511153
Abstract
In this report two brothers with a severe form of Peters' anomaly, i.e., primary dysgenesis mesodermalis of the cornea, are described. The third-degree consanguinity of the parents is an additional argument for the autosomal recessive inheritance of this condition.
摘要
在本报告中，描述了两名患有严重彼得斯异常（即角膜原发性中胚层发育不全）的兄弟。父母的三级血亲关系是支持这种疾病常染色体隐性遗传的另一个论据。
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