JOUBERT SYNDROME - A REVIEW

被引:224
作者
SARAIVA, JM
BARAITSER, M
机构
[1] INST CHILD HLTH, CLIN GENET & FETAL MED UNIT, 30 GUILFORD ST, LONDON WC1N 1EH, ENGLAND
[2] PAEDIAT HOSP, COIMBRA, PORTUGAL
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 43卷 / 04期
关键词
JOUBERT SYNDROME; JOUBERT-BOLTSHAUSER SYNDROME; RETINAL DYSTROPHY; VERMIS HYPOPLASIA;
D O I
10.1002/ajmg.1320430415
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We review 72 previously reported and 29 new patients with the possible diagnosis of Joubert syndrome. We define diagnostic criteria for this syndrome and present the data available in 94 patients that fulfill our criteria. We present the data regarding the clinical, neuroradiological, and ophthalmological manifestations and the prognosis of these 94 patients. We propose a classification of the patients with this diagnosis in 2 groups: those with retinal dystrophy and those without. Retinal dystrophy runs true in families and was never absent when renal cysts were reported.
引用
收藏
页码:726 / 731
页数:6
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