Sokolov B P, Prytkov A N, Tromp G, Knowlton R G, Prockop D J
Department of Biochemistry and Molecular Biology, Jefferson Institute of Molecular Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.
Hum Genet. 1991 Dec;88(2):125-9. doi: 10.1007/BF00206058.
Ehlers-Danlos syndrome (EDS) type I is a generalized connective tissue disorder, the major manifestations of which are soft, velvety hyperextensible skin and moderately severe joint hypermobility. The gene defect or defects causing EDS type I have not yet been defined, but previous observations suggested that the syndrome may be caused by mutations in the genes for type-I collagen (COL1A1 and COL1A2) or type-III collagen (COL3A1). Here, we performed linkage studies for these three genes in large Azerbaijanian family with EDS type I. Three polymorphisms in the COL3A1 gene, two in the COL1A1 gene, and one in the COL1A2 gene were tested using the polymerase chain reaction. The data obtained excluded linkage of any of the three genes to EDS type I in the family.
Ⅰ型埃勒斯-当洛综合征(EDS)是一种全身性结缔组织疾病,其主要表现为柔软、如天鹅绒般且过度伸展的皮肤以及中度严重的关节活动过度。导致Ⅰ型EDS的一个或多个基因缺陷尚未明确,但先前的观察表明,该综合征可能由Ⅰ型胶原蛋白(COL1A1和COL1A2)或Ⅲ型胶原蛋白(COL3A1)的基因突变引起。在此,我们对一个患有Ⅰ型EDS的阿塞拜疆大家族中的这三个基因进行了连锁研究。使用聚合酶链反应检测了COL3A1基因中的三个多态性、COL1A1基因中的两个多态性以及COL1A2基因中的一个多态性。所获得的数据排除了该家族中这三个基因中的任何一个与Ⅰ型EDS的连锁关系。