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

被引:34
作者
Atkinson, TP
Schäffer, AA
Grimbacher, B
Schroeder, HW
Woellner, C
Zerbe, CS
Puck, JM
机构
[1] NHGRI, Computat Biol Branch, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20892 USA
[2] NHGRI, Genet & Mol Biol branch, NIH, Bethesda, MD 20892 USA
[3] Univ Alabama, Dept Pediat, Birmingham, AL USA
[4] Univ Alabama, Dept Med, Birmingham, AL USA
[5] Univ Freiburg, Sch Med, Dept Rheumatol & Immunol, Freiburg, Germany
关键词
D O I
10.1086/323611
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 similar to 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.
引用
收藏
页码:791 / 803
页数:13
相关论文
共 66 条
  • [1] An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
    Aaltonen, J
    Bjorses, P
    Perheentupa, J
    HorelliKuitunen, N
    Palotie, A
    Peltonen, L
    Lee, YS
    Francis, F
    Hennig, S
    Thiel, C
    Lehrach, H
    Yaspo, ML
    [J]. NATURE GENETICS, 1997, 17 (04) : 399 - 403
  • [2] Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases
    Abreu, PC
    Greenberg, DA
    Hodge, SE
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (03) : 847 - 857
  • [3] AHONEN P, 1985, CLIN GENET, V27, P535, DOI 10.1111/j.1399-0004.1985.tb02037.x
  • [4] CLINICAL VARIATION OF AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) IN A SERIES OF 68 PATIENTS
    AHONEN, P
    MYLLARNIEMI, S
    SIPILA, I
    PERHEENTUPA, J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) : 1829 - 1836
  • [5] ADRENAL AND STEROIDAL CELL ANTIBODIES IN PATIENTS WITH AUTOIMMUNE POLYGLANDULAR DISEASE TYPE-I AND RISK OF ADRENOCORTICAL AND OVARIAN FAILURE
    AHONEN, P
    MIETTINEN, A
    PERHEENTUPA, J
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 64 (03) : 494 - 500
  • [6] Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome
    Barbesino, G
    Tomer, Y
    Concepcion, ES
    Davies, TF
    Greenberg, DA
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (09) : 3290 - 3295
  • [7] Automatic selection of loop breakers for genetic linkage analysis
    Becker, A
    Geiger, D
    Schäffer, AA
    [J]. HUMAN HEREDITY, 1998, 48 (01) : 49 - 60
  • [8] Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
    Bejjani, BA
    Lewis, RA
    Tomey, KF
    Anderson, KL
    Dueker, DK
    Jabak, M
    Astle, WF
    Otterud, B
    Leppert, M
    Lupski, JR
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (02) : 325 - 333
  • [9] Gene defect behind APECED:: a new clue to autoimmunity
    Björses, P
    Aaltonen, J
    Horelli-Kuitunen, N
    Yaspo, ML
    Peltonen, L
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (10) : 1547 - 1553
  • [10] IGG2/IGG4 SUBCLASS DEFICIENCY IN A PATIENT WITH CHRONIC MUCOCUTANEOUS CANDIDIASIS AND BRONCHIECTASES
    BRAGGER, C
    SEGER, RA
    AEPPLI, R
    HALLE, F
    HITZIG, WH
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1989, 149 (03) : 168 - 169