Literature DB >> 10766996

Novel mutation (E113X) of antithrombin III gene (AT3) in a woman with gestational recurrent thrombosis.

H Yamada1, N Hoshi, E H Kato, Y Ebina, T Kishida, T Sagawa, K Matsuno, S Fujimoto.   

Abstract

A 35-year-old Japanese woman with a low level (42-54%) of blood antithrombin (AT) III, experienced two induced abortions due to deep venous thrombosis at 8 weeks of gestation (GW) and cerebral thrombosis at 10 GW. The present pregnancy was successfully managed with intravenous administration of AT III (6,000-8,000 U/wk). Analysis of polymerase chain reaction (PCR)-single strand conformation polymorphism (SSCP) for exons 3A and 4 of the AT III gene (AT3) using her DNA revealed extra expansion bands with altered migration. The DNA sequencing demonstrated novel mutations in exon 3A of AT3: a G to T substitution at nucleotide position 5333 in codon GAG for Glu 113, causing a stop codon (E113X), and an A to T substitution at position 5338 in codon AAA for Lys 114, forming Asn (K114N). These novel mutations, especially E113X, in AT3 may be related to recurrent thrombosis in the pregnancy. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10766996

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Three case reports of inherited antithrombin deficiency in China: double novel missense mutations, a nonsense mutation and a frameshift mutation.

Authors:  Haoyu Deng; Wei Shen; Yi Gu; Xiong Ma; Jiwei Zhang; Lan Zhang
Journal:  J Thromb Thrombolysis       Date:  2012-08       Impact factor: 2.300

2.  Rare double heterozygous mutations in antithrombin underlie hereditary thrombophilia in a Chinese family.

Authors:  Haoyu Deng; Jiaquan Chen; Hui Xie; Yi Gu; Kai Yuan; Peng Wang; Wei Shen; Wei Liang; Hao Zhang; Jiwei Zhang; Jun Xie; Lan Zhang
Journal:  J Thromb Thrombolysis       Date:  2013-10       Impact factor: 2.300

  2 in total

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