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轻度脊椎骨骺发育不良(纳马夸兰型):与II型胶原基因COL2A1的遗传连锁关系。

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

作者信息

Sher C, Ramesar R, Martell R, Learmonth I, Tsipouras P, Beighton P

机构信息

Department of Human Genetics, University of Cape Town Medical School, South Africa.

出版信息

Am J Hum Genet. 1991 Mar;48(3):518-24.

Abstract

Namaqualand spondyloepiphyseal dysplasia (NSED) is a mild autosomal dominant form of spondyloepiphyseal dysplasia in which changes are maximal in the femoral capital epiphyses and the vertebral bodies. The condition is present in a large multigeneration South African family, and it is clinically important by virtue of severe progressive degenerative osteoarthropathy of the hip joint, which frequently necessitates prosthetic joint replacement in adulthood. Linkage studies using molecular markers have shown that the loci for the NSED and type II collagen genes are linked (LOD score 7.98 at a recombination fraction of .00).

摘要

纳马夸兰脊椎骨骺发育不良(NSED)是脊椎骨骺发育不良的一种轻度常染色体显性形式,其中股骨近端骨骺和椎体的变化最为明显。这种疾病存在于一个南非的大型多代家族中,由于髋关节严重进行性退行性骨关节炎,它在临床上具有重要意义,这种骨关节炎在成年期常常需要进行人工关节置换。使用分子标记的连锁研究表明,NSED基因座和II型胶原蛋白基因座是连锁的(重组率为0.00时,LOD分数为7.98)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f549/1682978/763d9d3db7be/ajhg00087-0088-a.jpg

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