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[Congenital deficiency of fibrin stabilizing factor [factor XIII)].

Authors
  • Blanckaert, D
  • Oueidat, I
  • Chelala, J
  • Loeuille, G A
  • Delepoulle, F
Type
Published Article
Journal
Pédiatrie
Publication Date
Jan 01, 1993
Volume
48
Issue
6
Pages
451–453
Identifiers
PMID: 8247644
Source
Medline
License
Unknown

Abstract

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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