Literature DB >> 11517424

An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.

T P Atkinson1, A A Schäffer, B Grimbacher, H W Schroeder, C Woellner, C S Zerbe, J M Puck.   

Abstract

We describe a large family in which a combination of chronic mucocutaneous candidiasis (fungal infections of the skin, nails, and mucous membranes) and thyroid disease segregate as an autosomal dominant trait with reduced penetrance. The family includes (a) four members with both candidiasis and thyroid disease, (b) five members, including one pair of phenotype-concordant MZ twins, with candidiasis only, and (c) three members with thyroid disease only. A whole-genome scan using DNA samples from 20 members of the family identified a candidate linkage region on chromosome 2p. By sampling additional individuals and genotyping supplementary markers, we established linkage to a region of approximately 15 cM bounded by D2S367 and D2S2240 and including seven adjacent markers consistent with linkage. With a penetrance estimate of.8, which was based on pedigree and affected status, the peak two-point LOD score was 3.70 with marker D2S2328, and the peak three-point LOD score was 3.82. This is the first linkage assignment of a dominant locus for mucocutaneous candidiasis.

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Year:  2001        PMID: 11517424      PMCID: PMC1226065          DOI: 10.1086/323611

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  61 in total

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Review 2.  Inborn errors of mucocutaneous immunity to Candida albicans in humans: a role for IL-17 cytokines?

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Review 5.  Inborn errors of human IL-17 immunity underlie chronic mucocutaneous candidiasis.

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6.  Deregulated production of protective cytokines in response to Candida albicans infection in patients with chronic mucocutaneous candidiasis.

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Review 8.  Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.

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9.  Chronic mucocutaneous candidiasis and primary hypothyroidism in two families.

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10.  An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis.

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