[Congenital deficiency of fibrin stabilizing factor [factor XIII)].
- Published Article
- Publication Date
Jan 01, 1993
The authors report a new case of congenital deficiency of fibrin stabilizing factor. The defect is transmitted as an autosomal recessive trait. The earliest symptom is umbilical bleeding when the cord separates. The diagnosis is confirmed by the rapid dispersion of the clot in urea 5 M or monochloroacetic acid.
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The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/8247644