Nevin N C, Thomas P S, Davis R I, Cowie G H
Regional Genetics Centre, Belfast City Hospital, Northern Ireland, United Kingdom.
Am J Med Genet. 1999 Feb 19;82(5):409-14. doi: 10.1002/(sici)1096-8628(19990219)82:5<409::aid-ajmg10>3.0.co;2-2.
We describe a 19-year-old woman with melorheostosis and osteopoikilosis (mixed sclerosing bone dysplasia). Her sister and mother had osteopoikilosis, but no evidence of melorheostosis. Isolated melorheostosis and melorheostosis with osteopoikilosis are sporadic disorders. Osteopoikilosis is an autosomal dominant trait. Mixed sclerosing bone dysplasia in a family with autosomal dominant osteopoikilosis raises the possibility that the two bone disorders may be related. This family and that of Butkus et al. [1997: Am J Med Genet 72:43-46] suggest that the melorheostosis could be due to a second mutation at the same locus as that which causes autosomal dominant osteopoikilosis.
我们描述了一名患有蜡油样骨病和骨斑点症(混合性硬化性骨发育异常)的19岁女性。她的姐姐和母亲患有骨斑点症,但无蜡油样骨病的证据。孤立性蜡油样骨病以及伴有骨斑点症的蜡油样骨病均为散发性疾病。骨斑点症是一种常染色体显性性状。在一个患有常染色体显性骨斑点症的家族中出现混合性硬化性骨发育异常,这增加了两种骨病可能相关的可能性。这个家族以及Butkus等人[1997年:《美国医学遗传学杂志》72:43 - 46]的家族提示,蜡油样骨病可能是由于与导致常染色体显性骨斑点症相同位点的第二次突变所致。