A Novel F45S SOD1 Mutation in Amyotrophic Lateral Sclerosis Coexisting with Bullous Pemphigoid

Citations

WEB OF SCIENCE

2
Citations

SCOPUS

2

초록

Background The coexistence of an autoimmune disease and amyotrophic lateral sclerosis (ALS) has led to the hypothesis that immune-mediated pathological mechanisms are overlapping in the two diseases. We report herein a rare coexistence of bullous pemphigoid (BP) in a novel mutation (F45S) of the gene encoding Cu/Zn superoxide dismutase (SOD1) in an ALS patient, and discuss a role for the SOD1 mutation in this unusual overlap. Case Report A 57-year-old male with familial ALS, including vesicles and tense bullae on erythematous bases, was diagnosed with BP. Direct immunofluorescence revealed deposits of C3 and immunoglobulin G in the basement membrane zone. Direct sequencing of SOD1 in the patient revealed a novel mutation (c.137T>C; F45S). Conclusions We report a novel SOD1 mutation in ALS, which was combined with BR This novel SOD1 mutation could affect the phenotype of a combined autoimmune disease and matrix metalloproteinase-9. There may therefore be common factors linking BP and ALS with the SOD1 mutation.

키워드

amyotrophic lateral sclerosisbullous pemphigoidsuperoxide dismutaseautoimmunityDISEASES
제목
A Novel F45S SOD1 Mutation in Amyotrophic Lateral Sclerosis Coexisting with Bullous Pemphigoid
저자
Oh, Seong-ilHong, Jeong HoChoi, Byung WooOh, Ki-WookPark, Chan KumKwon, Min-JungKi, Chang-SeokKo, Joo YeonKim, Seung Hyun
DOI
10.3988/jcn.2015.11.4.390
발행일
2015-10
유형
Article
저널명
Journal of Clinical Neurology
11
4
페이지
390 ~ 394

파일 다운로드