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KMID : 0384119900100020365
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Korean Journal of Clinical Pathology
1990 Volume.10 No. 2 p.365 ~ p.368
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A Case of congenital Afibrinogenemia
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C. H. Lee
J. W. Lee/H. S. Kim/K. S. Song
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Abstract
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Congenital afibrinogenemia is a very rare hereditary coagulation disorder characterized by decreased fibrinogen synthesis and bleeding episode. It was fist mentioned by Rabe and Salomon in 1920, after that time about 150 cases have been reported until 1985. Recently, we experienced a case of newborn who was suffering from umbilical bleeding, and it is considered that this is the second afibrinogenemic case in Korea. So, we reported this case with the review of articles.
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