Butkus C E, Michels V V, Lindor N M, Cooney W P
Department of Internal Medicine, University of Rochester, New York, USA.
Am J Med Genet. 1997 Oct 3;72(1):43-6. doi: 10.1002/(sici)1096-8628(19971003)72:1<43::aid-ajmg9>3.0.co;2-w.
We report on a 40-year-old woman with melorheostosis who also had radiographic findings of generalized osteopoikilosis. Three of her sibs have osteopoikilosis, but none of them have melorheostosis. Several cases of "mixed sclerosing bone dysplasia" have been described previously, and all have been sporadic. Isolated melorheostosis without osteopoikilosis is also generally a sporadic condition, but osteopoikilosis has been described as an autosomal-dominant trait. The finding of mixed sclerosing bone dysplasia in a family with osteopoikilosis suggests that the melorheostotic component of this disorder may be due to a second mutation at the same locus that causes isolated familial osteopoikilosis.
我们报告了一名40岁患有蜡油样骨病的女性,其影像学检查还发现有全身点状骨病。她的三个兄弟姐妹患有点状骨病,但均无蜡油样骨病。先前已描述过几例“混合性硬化性骨发育异常”病例,均为散发性。孤立性蜡油样骨病而无点状骨病通常也是散发性疾病,但点状骨病被描述为常染色体显性性状。在一个患有点状骨病的家族中发现混合性硬化性骨发育异常提示,这种疾病的蜡油样骨病成分可能是由于在导致孤立性家族性点状骨病的同一基因座发生了第二次突变。