Document Detail


Percutaneous coronary intervention in a case of afibrinogenemia.
MedLine Citation:
PMID:  24570509     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Congenital afibrinogenemia is a rare autosomic recessive blood disorder. A 30-year-old lady, known to have congenital afibrinogenemia, presented with acute anterior myocardial infarction. We managed her with dual antiplatelet therapy and atorvastatin, but her chest pain did not subside and she was transferred to the catheterization laboratory. A proximal left anterior descending artery occlusion was crossed with a floppy wire. Angioplasty was performed successfully with a bare metal stent, and her symptoms resolved completely.
Authors:
Homa Falsoleiman; Mehdi Hasanzadeh Daloee; Mashalla Dehghani; Atoosheh Rohani; Baktash Bayani
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Asian cardiovascular & thoracic annals     Volume:  21     ISSN:  1816-5370     ISO Abbreviation:  Asian Cardiovasc Thorac Ann     Publication Date:  2013 Jun 
Date Detail:
Created Date:  2014-02-26     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9503417     Medline TA:  Asian Cardiovasc Thorac Ann     Country:  England    
Other Details:
Languages:  eng     Pagination:  358-9     Citation Subset:  IM    
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