先天性凝血因子II、VII、IX和X联合缺乏症。病例报告。 - Suppr

Congenital combined deficiency of coagulation factors II, VII, IX and X. Report of a case.

作者信息

McMillan C W, Roberts H R

出版信息

N Engl J Med. 1966 Jun 9;274(23):1313-5. doi: 10.1056/NEJM196606092742309.

DOI:10.1056/NEJM196606092742309

PMID:5936414

Abstract

摘要

相似文献

Congenital combined deficiency of coagulation factors II, VII, IX and X. Report of a case.

N Engl J Med. 1966 Jun 9;274(23):1313-5. doi: 10.1056/NEJM196606092742309.

[Experimental models of human congenital coagulation defects].

Probl Gematol Pereliv Krovi. 1981 Nov;26(11):41-4.

Congenital bleeding disorders of the vitamin K-dependent clotting factors.

Vitam Horm. 2008;78:281-374. doi: 10.1016/S0083-6729(07)00014-3.

[Proceedings: Congenital deficiencies of factors II, V, VII and X].

Minerva Pediatr. 1973 Dec 15;25(43):1933-42.

[Inborn metabolism errors LV. Congenital "hypoprothrombinemia": Deficiency of II, VII or X].

Ugeskr Laeger. 1976 Jun 7;138(24):1462-5.

Congenital hypoprothrombinemia. A case report.

Haematol Lat. 1969 Jan-Mar;12(1):77-89.

Characterization of a variant prothrombin in a patient congenitally deficient in factors II, VII, IX and X.

Br J Haematol. 1980 Mar;44(3):461-9. doi: 10.1111/j.1365-2141.1980.tb05916.x.

[A new case of homozygous congenital factor VII deficiency. Associated factor X deficiency in some members of the family].

Ann Pediatr (Paris). 1971 Dec 14;18(12):817-23.

Congenital "hypoprothrombinemias". Deficiency of factors II, VII, and X.

Med Clin North Am. 1972 Jan;56(1):127-32. doi: 10.1016/s0025-7125(16)32428-2.

[The P.P.S.B. coagulant fraction].

Nouv Presse Med. 1975 Oct 25;4(36):2581-4.

引用本文的文献

Vitamin K-Dependent Protein Activation: Normal Gamma-Glutamyl Carboxylation and Disruption in Disease.

Int J Mol Sci. 2022 May 20;23(10):5759. doi: 10.3390/ijms23105759.

Suspected vitamin K-dependent coagulation factor deficiency in pregnancy: A case report.

Case Rep Womens Health. 2022 Apr 27;34:e00416. doi: 10.1016/j.crwh.2022.e00416. eCollection 2022 Apr.

γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins.

Blood. 2021 Jan 28;137(4):533-543. doi: 10.1182/blood.2020006329.

Molecular basis of the first reported clinical case of congenital combined deficiency of coagulation factors.

Blood. 2017 Aug 17;130(7):948-951. doi: 10.1182/blood-2017-05-782367. Epub 2017 Jul 5.

Characterization of vitamin K-dependent carboxylase mutations that cause bleeding and nonbleeding disorders.

Blood. 2016 Apr 14;127(15):1847-55. doi: 10.1182/blood-2015-10-677633. Epub 2016 Jan 12.

Fibroblast involvement in soft connective tissue calcification.

Front Genet. 2013 Mar 5;4:22. doi: 10.3389/fgene.2013.00022. eCollection 2013.

Hereditary combined deficiency of the vitamin K-dependent clotting factors.

Orphanet J Rare Dis. 2010 Jul 14;5:21. doi: 10.1186/1750-1172-5-21.

Familial deficiency of vitamin K-dependent clotting factors.

Haemophilia. 2008 Nov;14(6):1209-13. doi: 10.1111/j.1365-2516.2008.01853.x.

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency.

Blood. 2006 Sep 15;108(6):1925-31. doi: 10.1182/blood-2005-12-010660. Epub 2006 May 23.

Studies on a family with combined functional deficiencies of vitamin K-dependent coagulation factors.

J Clin Invest. 1982 Jun;69(6):1253-60. doi: 10.1172/jci110564.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Congenital combined deficiency of coagulation factors II, VII, IX and X. Report of a case.

作者信息

出版信息

相似文献

引用本文的文献

文献AI研究员

用中文搜PubMed

文档翻译

Suppr 超能文献

相似文献

引用本文的文献