These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Ochronosis of the Entire Aortic Root in Alkaptonuria;Report of a Case].
    Author: Komatsu H, Kanamitsu H, Mohri M.
    Journal: Kyobu Geka; 2020 Nov; 73(12):1041-1044. PubMed ID: 33268759.
    Abstract:
    Alkaptonuria is a rare hereditary disorder of phenylalanine and tyrosine metabolism, which results in ochronosis of cardiovascular structures including valves, aortic intima, and coronary arteries. Aortic valve disease is the most frequently reported cardiac sequela of alkaptonuria. We report a case of 77-year-old woman with known alkaptonuria who underwent aortic valve replacement for severe aortic stenosis. Operative findings showed impressive ochronosis of the aortic valve and the aortic intima. The post-operative course was uneventful and she was discharged 25 days after the surgery.
    [Abstract] [Full Text] [Related] [New Search]