Literature DB >> 22367836

Autoimmune polyendocrine syndrome-3 in a patient with late-onset multiple sclerosis.

Hiroaki Yokote1, Miki Nagasawa, Masahiko Ichijo, Takeshi Amino, Hiroto Fujigasaki.   

Abstract

We present here the rare case of a 73-year-old patient with very late-onset multiple sclerosis who developed autoimmune polyendocrine syndrome (APS)-3. Despite only a few reports describing the association between multiple sclerosis and APS, both of these diseases have been shown to be associated with HLA-DR4. Intriguingly, the HLA genotype profile of this patient included HLA-DR4 which, fine mapped to the DRB1*0405-DQA1*0303-DQB1*0401 extended haplotype, reported to be a susceptibility haplotype for APS-3 in Japan. This unique genetic background might explain the clinical picture of this patient.

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Year:  2012        PMID: 22367836     DOI: 10.1097/NRL.0b013e318248ea2a

Source DB:  PubMed          Journal:  Neurologist        ISSN: 1074-7931            Impact factor:   1.398


  3 in total

1.  Unusual case of anti-N-methyl-D-aspartic acid-receptor (NMDA-R) encephalitis and autoimmune polyglandular syndrome (APS).

Authors:  Simona Frunza-Stefan; Hilary B Whitlatch; Gautam G Rao; Rana Malek
Journal:  BMJ Case Rep       Date:  2018-05-02

2.  Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review.

Authors:  Michael Apolinario; Aaron Brussels; Curtiss B Cook; Shaun Yang
Journal:  Clin Case Rep       Date:  2022-02-04

Review 3.  Autoimmune polyglandular syndrome type III associated with antineutrophil cytoplasmic autoantibody-mediated crescentic glomerulonephritis: A case report and literature review.

Authors:  Shiyuan Tian; Baofeng Xu; Ziwei Liu; Rui Liu
Journal:  Medicine (Baltimore)       Date:  2020-02       Impact factor: 1.817

  3 in total

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