Melorheostosis may originate as a type 2 segmental manifestation of osteopoikilosis

被引:19
作者
Happle, R [1 ]
机构
[1] Univ Marburg, Dept Dermatol, D-35033 Marburg, Germany
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2004年 / 125A卷 / 03期
关键词
melorheostosis; osteopoikilosis; Buschke-Ollendorff syndrome; mixed sclerosing bone dysplasia; loss of heterozygosity; type 2 segmental manifestation of autosomal dominant traits;
D O I
10.1002/ajmg.a.20454
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Melorheostosis is a non-hereditary disorder involving the bones in a segmental pattern, whereas osteopoikilosis is a rather mild disseminated bone disorder inherited as an autosomal dominant trait. Interestingly, melorheostosis and osteopoikilosis may sometimes occur together. In analogy to various autosomal dominant skin disorders for which a type 2 segmental manifestation has been postulated, melorheostosis may be best explained in such cases as a type 2 segmental osteopoikilosis, resulting from early loss of the corresponding wild type allele at the gene locus of this autosomal dominant bone disorder. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:221 / 223
页数:3
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