Literature DB >> 10826862

Takayasu's arteritis concurrent with Marfan syndrome--a case report.

H J Baek1, K C Shin, Y J Lee, S W Kang, E B Lee, Y W Song.   

Abstract

Marfan syndrome (MS) is a dominantly inherited connective tissue disorder characterized by arachnodactyly, tall stature, the presence of aortic aneurysm, and lens dislocation. Takayasu's arteritis (TA) is a chronic vasculitis that primarily affects the aorta and its branches. The authors report the first case of TA in a patient with MS. The simultaneous presence of TA and MS could be a coincidence, however; the pathogenesis of TA might be linked with autoimmunity induced by abnormal extracellular matrix protein derived from the genetic mutations in MS.

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Year:  2000        PMID: 10826862     DOI: 10.1177/000331970005100512

Source DB:  PubMed          Journal:  Angiology        ISSN: 0003-3197            Impact factor:   3.619


  1 in total

1.  Esophageal Artery Pseudoaneurysm and Takayasu Arteritis in a Patient with Autosomal Dominant Polycystic Kidney Disease.

Authors:  Hyunsuk Kim; Yeonsil Yu; Kwang Eon Shim; Jin Eop Kim; Junga Koh; Jong-Woo Yoon; Curie Ahn; Yun Kyu Oh
Journal:  Electrolyte Blood Press       Date:  2018-06-30
  1 in total

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