| Literature DB >> 10726006 |
Abstract
While patients with hereditary muscular disorder are more sedentary and believed to be at risk of thrombosis, there is little literature on thrombosis associated with hereditary muscular disorder. We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.Entities:
Mesh:
Substances:
Year: 1999 PMID: 10726006 DOI: 10.1177/107602969900500308
Source DB: PubMed Journal: Clin Appl Thromb Hemost ISSN: 1076-0296 Impact factor: 2.389