Retinitis pigmentosa in a young man with Noonan syndrome: Further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?

被引:0
|
作者
Lorenzetti, ME
Fryns, JP
机构
[1] CATHOLIC UNIV LEUVEN,CTR HUMAN GENET,B-3000 LOUVAIN,BELGIUM
[2] UNIV PARMA,DEPT PEDIAT,GENET CTR,I-43100 PARMA,ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 65卷 / 02期
关键词
cardio-facio-cutaneous (CFC) syndrome; Noonan syndrome; retinitis pigmentosa; autosomal dominant inheritance;
D O I
10.1002/(SICI)1096-8628(19961016)65:2<97::AID-AJMG1>3.0.CO;2-R
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a young man with Noonan syndrome (NS) and retinitis pigmentosa. As far as we know, retinitis pigmentosa has not been reported in NS. However, in the 3 cardio-facio-cutaneous syndrome (CFC) patients in whom electroretinographic studies were performed, retinal anomalies have been found. In addition, decreased vision, refractive errors, strabismus, and optic disc anomalies were reported in CFC patients. This observation suggests that NS and CFC are variable manifestations of the same entity. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:97 / 99
页数:3
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