| Literature DB >> 1333307 |
K Deguchi1, T Tsukada, E Iwasaki, H Wada, S Murashima, M Miyazaki, S Shirakawa.
Abstract
We report a 31-year-old female who had repeated thrombosis and was diagnosed as having congenital homozygous protein C deficiency based on decreased protein C antigen and activity, and the findings of family history. This patient had shown no symptom of thrombosis until the age of 27 years, when she had cerebral infarction as the first symptom. Low molecular weight heparin was useful for disseminated intravascular coagulation (DIC) that complicated protein C deficiency in this patient.Entities:
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Year: 1992 PMID: 1333307 DOI: 10.2169/internalmedicine.31.922
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271