| Literature DB >> 9220135 |
G Fecteau1, J G Zinkl, B P Smith, S O'Neil, S Smith, S Klopfer.
Abstract
Hereditary fibrinogen deficiency is a rare condition in all species. Measurement of plasma fibrinogen should indicate low levels. Specific factor assays and pedigree analysis are essential in establishing a definitive diagnosis of the hereditary deficiency. Differentiation between afibrinogenemia, hypofibrinogenemia, and dysfibrinogenemia requires sophisticated techniques and assistance from a specialized laboratory.Entities:
Mesh:
Year: 1997 PMID: 9220135 PMCID: PMC1576739
Source DB: PubMed Journal: Can Vet J ISSN: 0008-5286 Impact factor: 1.008