POSSIBLE NEW TYPE OF ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES - OFDS TYPE-(VIII)

被引:35
作者
GURRIERI, F
SAMMITO, V
RICCI, B
IOSSA, M
BELLUSSI, A
NERI, G
机构
[1] UNIV CATTOLICA SACRO CUORE, A GEMELLI SCH MED, IST GENET UMANA, LARGO F VITO 1, I-00168 ROME, ITALY
[2] UNIV CATTOLICA SACRO CUORE, A GEMELLI SCH MED, IST CLIN OCULIST, I-00168 ROME, ITALY
[3] OSPED S CAMILLO ROMA, SERV RADIOL, ROME, ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 42卷 / 06期
关键词
ORAL-FACIAL-DIGITAL SYNDROME TYPE-VIII; HALLUX DUPLICATION; RETINOCHOROIDEAL LACUNAE;
D O I
10.1002/ajmg.1320420608
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The most recent classification of the oral-facial-digital syndromes (OFDS) includes 7 types distinguishable by different clinical signs. We describe 2 brothers presenting oral, facial, and digital anomalies and an additional manifestation consisting of specific retinal abnormalities, i.e., retinochoroidal lacunae of colobomatous origin. Our patients may be affected with a new type of OFDS, i.e., OFDS type VIII, characterized by eye abnormalities in addition to other manifestations that partially overlap with those of OFDS type II. Given that there are 2 affected brothers, we cannot distinguish between autosomal and X-linked recessive inheritance.
引用
收藏
页码:789 / 792
页数:4
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