A FAMILIAL FACTOR-XIII SUBUNIT-B DEFICIENCY

被引:70
作者
SAITO, M
ASAKURA, H
YOSHIDA, T
ITO, K
OKAFUJI, K
YOSHIDA, T
MATSUDA, T
机构
[1] FUKUI SAISEIKAI HOSP,DEPT INTERNAL MED,FUKUI,JAPAN
[2] KANAZAWA UNIV,SCH MED,CENT CLIN LAB,KANAZAWA,ISHIKAWA 920,JAPAN
关键词
D O I
10.1111/j.1365-2141.1990.tb02585.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 32‐year‐old woman with a bleeding tendency born of a consanguineous marriage, was found to have factor XIII subunit B deficiency. An abnormally low level of factor XIII activity was initially noticed and this finding led to further studies of the proband and her family. The notable features were: undetectable subunit B of factor XIII in the proband and her brother and reduced levels of subunit B, 34–52%, in her parents and children. The proband's brother had a markedly decreased level of subunit A protein. The level of factor XIII subunit A in platelets of the proband was normal. The half‐life of subunit A determined from the disappearance curve of infused factor XIII subunit A concentrate was approximately 3 d and this is the shortest estimate of the half‐life of factor XIII to date. From these results, it is suggested that subunit A is unstable in plasma deficient in subunit B and subunit B stabilizes the A protein. This is the first report of congenital deficiency of factor XIII subunit B and this disorder is thought to be inherited as an autosomal recessive trait. Copyright © 1990, Wiley Blackwell. All rights reserved
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页码:290 / 294
页数:5
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