THE MANY FACES OF ORAL-FACIAL-DIGITAL SYNDROME

被引:4
|
作者
Sukarova-Angelovska, E. [1 ]
Angelkova, N. [2 ]
Palcevska-Kocevska, S. [3 ]
Kocova, M. [1 ]
机构
[1] Fac Med, Pediat Clin, Dept Endocrinol & Genet, Skopje 1000, Macedonia
[2] Pediat Clin, Dept Neurol, Skopje, Macedonia
[3] Pediat Clin, Dept Neonatol, Skopje, Macedonia
关键词
Oral-facial-digital (OFD) syndrome; Oral cleft; Polydactyly; Ciliopathy; Genetic and clinical heterogeneity; SYNDROME TYPE-IV; MOHR-SYNDROME; PRENATAL-DIAGNOSIS; SYNDROME TYPE-1; OFD SYNDROME; SPECTRUM; EXPRESSION; ANOMALIES; FEATURES; VARIANT;
D O I
10.2478/v10034-012-0006-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The oral-facial-digital (OFD) syndrome is a heterogeneous group of abnormalities that share anomalies of the oral cavity, face and digits of hands and feet. On the basis of other anomalies of brain, kidneys, limbs, eyes and other organs, at least 13 subgroups have been described. We here describe four unrelated patients with this syndrome, who have the typical facial, oral and digital anomalies and also anomalies of other organs and systems. Facial features, digital malformations, as well as the existence of additional malformations all of which can be classified into different subgroups. The report points out the difficulty in delineation of the subtypes of OFD syndrome because of the overlapping features between OFD subgroups.
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页码:37 / 44
页数:8
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