Literature DB >> 10706361

Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome.

P J Ferguson1, S H Blanton, F T Saulsbury, M J McDuffie, V Lemahieu, J M Gastier, U Francke, S M Borowitz, J L Sutphen, T E Kelly.   

Abstract

The clinical findings of a kindred with an X-linked disorder are characterized by autoimmune polyendocrinopathy, enteropathy with villous atrophy, chronic dermatitis, and variable immunodeficiency. Linkage analysis was performed on 20 members of the affected kindred to determine the location of the responsible locus. Informative recombinations limited the region to an approximate 20 cM interval bordered by DXS1055 and DXS1196/DXS1050. Multipoint analysis generated a lod score >3 for the region contained between DXS8024 and DXS8031. The candidate region includes the Wiskott-Aldrich syndrome (WAS) locus. Evaluation of the Wiskott-Aldrich syndrome protein gene by single strand conformational analysis, heteroduplex analysis, and direct sequencing of the 12 exons in an affected male and two carrier females revealed no abnormalities. We conclude that this kindred has an X-linked disorder, distinct from WAS, that results in autoimmunity and variable immunodeficiency. The responsible locus maps to the pericentromeric region Xp11.23 to Xq21.1.

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Year:  2000        PMID: 10706361     DOI: 10.1002/(sici)1096-8628(20000228)90:5<390::aid-ajmg9>3.0.co;2-m

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  19 in total

1.  Escape from tolerance in the human X-linked autoimmunity-allergic disregulation syndrome and the Scurfy mouse.

Authors:  D D Patel
Journal:  J Clin Invest       Date:  2001-01       Impact factor: 14.808

2.  Medium-term survival without haematopoietic stem cell transplantation in a case of IPEX: insights into nutritional and immunosuppressive therapy.

Authors:  Andrea Taddio; Elena Faleschini; Erica Valencic; Marilena Granzotto; Alberto Tommasini; Loredana Lepore; Marino Andolina; Egidio Barbi; Alessandro Ventura
Journal:  Eur J Pediatr       Date:  2007-01-05       Impact factor: 3.183

3.  X-chromosome inactivation analysis in a female carrier of FOXP3 mutation.

Authors:  A Tommasini; S Ferrari; D Moratto; R Badolato; M Boniotto; D Pirulli; L D Notarangelo; M Andolina
Journal:  Clin Exp Immunol       Date:  2002-10       Impact factor: 4.330

4.  The forkhead transcription factor, FOXP3: a critical role in male fertility in mice.

Authors:  Jake S Jasurda; Deborah O Jung; Erin D Froeter; David B Schwartz; Torin D Hopkins; Corrie L Farris; Stacey McGee; Prema Narayan; Buffy S Ellsworth
Journal:  Biol Reprod       Date:  2014-01-09       Impact factor: 4.285

Review 5.  Monogenic autoimmunity.

Authors:  Mickie H Cheng; Mark S Anderson
Journal:  Annu Rev Immunol       Date:  2012-01-06       Impact factor: 28.527

6.  JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome.

Authors:  T A Chatila; F Blaeser; N Ho; H M Lederman; C Voulgaropoulos; C Helms; A M Bowcock
Journal:  J Clin Invest       Date:  2000-12       Impact factor: 14.808

7.  Are mouse models of human mycobacterial diseases relevant? Genetics says: 'yes!'.

Authors:  Alexander S Apt
Journal:  Immunology       Date:  2011-10       Impact factor: 7.397

Review 8.  Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.

Authors:  R S Wildin; S Smyk-Pearson; A H Filipovich
Journal:  J Med Genet       Date:  2002-08       Impact factor: 6.318

Review 9.  FOXP3: genetic and epigenetic implications for autoimmunity.

Authors:  Hiroto Katoh; Pan Zheng; Yang Liu
Journal:  J Autoimmun       Date:  2013-01-11       Impact factor: 7.094

Review 10.  IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.

Authors:  Hans D Ochs; Eleonora Gambineri; Troy R Torgerson
Journal:  Immunol Res       Date:  2007       Impact factor: 2.829

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