Ghadami M, Makita Y, Yoshida K, Nishimura G, Fukushima Y, Wakui K, Ikegawa S, Yamada K, Kondo S, Niikawa N, Tomita H a
Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki 852-8523, Japan.
Am J Hum Genet. 2000 Jan;66(1):143-7. doi: 10.1086/302728.
Camurati-Engelmann disease (CED [MIM 131300]), or progressive diaphyseal dysplasia, is an autosomal dominant sclerosing bone dysplasia characterized by progressive bone formation along the periosteal and endosteal surfaces at the diaphyseal and metaphyseal regions of long bones and cranial hyperostosis, particularly at the skull base. The gene for CED, or its chromosomal localization, has not yet been identified. We performed a genomewide linkage analysis of two unrelated Japanese families with CED, in which a total of 27 members were available for this study; 16 of them were affected with the disease. Two-point linkage analysis revealed a maximum LOD score of 7.41 (recombination fraction.00; penetrance 1.00) for the D19S918 microsatellite marker locus. Haplotype analysis revealed that all the affected individuals shared a common haplotype observed, in each family, between D19S881 and D19S606, at chromosome 19q13.1-q13.3. These findings, together with a genetic distance among the marker loci, indicate that the CED locus can be assigned to a 15.1-cM segment between D19S881 and D19S606.
卡穆拉蒂 - 恩格尔曼病(CED [MIM 131300]),即进行性骨干发育异常,是一种常染色体显性遗传性硬化性骨发育异常疾病,其特征为长骨干骺端和骨干区域的骨膜和骨内膜表面进行性骨形成以及颅骨增生,尤其是颅底部位。CED的致病基因或其染色体定位尚未确定。我们对两个患CED的无关日本家族进行了全基因组连锁分析,共有27名成员参与本研究,其中16人患病。两点连锁分析显示,D19S918微卫星标记位点的最大对数优势分数为7.41(重组率为0.00;外显率为1.00)。单倍型分析表明,所有患病个体在19号染色体q13.1 - q13.3区域共享一个常见单倍型,该单倍型在每个家族中均位于D19S881和D19S606之间。这些发现,连同标记位点之间的遗传距离,表明CED基因座可定位于D19S881和D19S606之间15.1厘摩的区域。