Literature DB >> 22506295

Successful liver transplantation for a child with life-threatening recurrent bleeding episodes due to congenital factor X deficiency: a case report.

S H Bang1, S H Oh, K M Kim, S M Song, J J Seo, H W Yoo, T H Kim, D Y Kim, S G Lee.   

Abstract

Factor X (FX) deficiency is a rare, autosomal-recessive coagulation disorder. Diagnosis can be confirmed by a factor X assay. Although fresh frozen plasma and prothrombin complex concentrates have been used as a temporary treatment of bleeding symptoms and preparation for surgery, frequent transfusion has its risk and prothrombin complex is not available in Korea. We report the first pediatric case of successful liver transplantation for the correction of a severe congenital FX deficiency in a child with recurrent life-threatening hemorrhagic episodes.

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Year:  2012        PMID: 22506295     DOI: 10.1016/j.transproceed.2012.01.075

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  2 in total

1.  Factor X heterozygous mutation in a patient with potential risk of bleeding: A case report.

Authors:  Kotaro Arita; Hideki Niimi; Nana Yamagishi; Tomohiro Ueno; Isao Kitajima; Toshiro Sugiyama
Journal:  Medicine (Baltimore)       Date:  2018-06       Impact factor: 1.889

2.  Pediatric split liver transplantation for congenital factor X deficiency: first 10-year follow-up of a case with portal vein stenting.

Authors:  Jung-Man Namgoong; Shin Hwang; Dae-Yeon Kim; Tae-Yong Ha; Gi-Won Song; Dong-Hwan Jung; Kyung Mo Kim; Seak Hee Oh
Journal:  Korean J Transplant       Date:  2021-03-12
  2 in total

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