el-Shanti H, Murray J C, Semina E V, Beutow K H, Scherpbier T, al-Alami J
Department of Pediatrics, Jordan University of Science and Technology, Irbid, Jordan.
Eur J Hum Genet. 1998 May-Jun;6(3):251-6. doi: 10.1038/sj.ejhg.5200187.
Progressive pseudorheumatoid dysplasia is an autosomal recessive skeletal dysplasia with radiographic changes in the spine similar to Spondyleopiphyseal dysplasia tarda and clinical, though not radiographic resemblance to rheumatoid arthritis. About two-thirds of the reported patients are of Arabic and Mediterranean origin which reflects the relative high incidence in this population. We performed homozygosity mapping utilising the DNA pooling approach to map progressive pseudorheumatoid dysplasia to a chromosomal region on the long arm of chromosome 6. We examined a possible candidate gene in the same region of linkage, namely COL10A1, for alterations in this disorder. We did not identify any mutations in our family, but did not totally exclude COL10A1 gene from being the disease-causing gene.
进行性假类风湿性发育不良是一种常染色体隐性遗传性骨骼发育不良,其脊柱的影像学改变类似于迟发性脊椎骨骺发育不良,临床症状虽与类风湿性关节炎不同,但影像学表现相似。约三分之二的报告患者来自阿拉伯和地中海地区,这反映了该人群中相对较高的发病率。我们采用DNA池化方法进行纯合性定位,将进行性假类风湿性发育不良定位到6号染色体长臂上的一个染色体区域。我们检查了该连锁区域内的一个可能候选基因,即COL10A1,以寻找该疾病的相关改变。我们在我们的家系中未发现任何突变,但并未完全排除COL10A1基因是致病基因的可能性。