Molecular genetic analysis of a family with a history of Hodgkin's disease and dyschondrosteosis.

D A Gokhale, D G Evans, D Crowther, P Woll, C J Watson, S P Dearden, W D Fergusson, R F Stevens, G M Taylor

    Research output: Contribution to journalArticlepeer-review

    Abstract

    We describe a family in which two sisters with the autosomal dominant skeletal dysplasia, Leri-Weill dyschondrosteosis (LWD), developed Hodgkin's disease (HD) in late adolescence. In a preliminary attempt to identify HD susceptibility gene(s), HLA-typing and linkage analysis were carried out in the family. Using HLA molecular typing, both sisters were found to have inherited a variant of the HD-susceptibility allele, DPB1*0301, known as DPB1*2001. Following a previous report of a constitutional chromosome translocation (t(2q;8p)) in a family with LWD, preliminary linkage studies were carried out using chromosome 2q and 8p molecular markers. Regions covered by 7/10 chromosome 2 markers and 4/8 chromosome 8 markers were excluded as the location of a candidate LWD gene. Given the rarity of LWD and HD, their simultaneous occurrence is unlikely to have been due to chance. We suggest that a mutation in the LWD gene itself, or a gene closely linked to it, perhaps acting with increased susceptibility to infection conferred by DPB1*2001, resulted in HD in the two sisters.
    Original languageEnglish
    JournalLeukemia
    Volume9
    Issue number5
    Publication statusPublished - May 1995

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