| Literature DB >> 22367836 |
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.Entities:
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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