Literature DB >> 16424563

Hereditary coagulation factor X deficiency.

A Kumar1, K L Mishra, A Kumar1, D Mishra.   

Abstract

Stuart Prower factor (Factor X) deficiency is a rare hereditary autosomal recessive coagulation disorder. We have come across three cases in the course of last 20 years at our institute. These patients presented with prolonged bleeding after minor trauma, epistaxis, subcutaneous bluish black nodules and two of them presented with history of consanguinity in parents. Hematological findings in correlation with clinical manifestations revealed severe factor X deficiency.

Entities:  

Mesh:

Year:  2005        PMID: 16424563

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  5 in total

1.  Rare case of combined factor V and factor X deficiency in pregnancy: presenting as secondary postpartum haemorrhage in first pregnancy and successful outcome in second pregnancy.

Authors:  Aniket Kakade; Tushar Panchanadikar; Yashwant Kulkarni
Journal:  Obstet Med       Date:  2013-05-03

2.  Factor X deficiency: a rare cause of puberty menorrhagia.

Authors:  Virender Singh; Tania Kakkar; Sanjeev K Digra; Manisha Kakkar
Journal:  Indian J Pediatr       Date:  2012-06-14       Impact factor: 1.967

3.  An analysis of 8 cases of factor X deficiency.

Authors:  Nilam M Shah; Ashwin P Patel
Journal:  Indian J Hematol Blood Transfus       Date:  2008-05-01       Impact factor: 0.900

4.  Surgical treatment for a paraplegic patient induced by congenital factor X deficiency.

Authors:  Weicheng Lin; Jing Zhou; Tianbing Wang; Peixun Zhang
Journal:  Int J Clin Exp Med       Date:  2015-08-15

5.  Membranoproliferative glomerulonephritis and a rare bleeding disorder: Factor X deficiency.

Authors:  T Basturk; E Ahbap; B Eroglu Kesim; M Yılmaz; Y Koç; T Sakacı; A Unsal
Journal:  Int Urol Nephrol       Date:  2010-09-23       Impact factor: 2.370

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.