Literature DB >> 9695984

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients.

F Peyvandi1, P M Mannucci, M Lak, M Abdoullahi, S Zeinali, R Sharifian, D Perry.   

Abstract

The spectrum of the clinical manifestations of congenital factor X deficiency was studied in 32 Iranian patients. The most frequent symptom was epistaxis, which occurred in 72% of patients, with all degrees of deficiency. Other mucosal haemorrhages (e.g. haematuria, gastrointestinal bleeding) were less frequent and occurred mainly in patients with unmeasurable factor X. Menorrhagia occurred in half of the women of reproductive age. Soft tissue bleeding occurred in two-thirds of the patients; spontaneous haematomas and haemarthroses led to severe arthropathy in five patients. Bleeding from the umbilical stump was an unexpected finding in nine patients. This study demonstrated that the bleeding tendency of factor X deficiency is severe and correlates with factor levels.

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Year:  1998        PMID: 9695984     DOI: 10.1046/j.1365-2141.1998.00806.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  15 in total

1.  Inherited Factor X (Stuart-Prower Factor) deficiency and its management.

Authors:  T Chatterjee; J Philip; Velu Nair; R S Mallhi; Hemant Sharma; P Ganguly; A K Biswas
Journal:  Med J Armed Forces India       Date:  2014-04-03

2.  Factor X M402T: a homozygous missense mutation identified as the cause of cross-reacting material-reduced deficiency.

Authors:  Yushi Chikasawa; Keiko Shinozawa; Kagehiro Amano; Kyoichi Ogata; Takeshi Hagiwara; Takashi Suzuki; Hiroshi Inaba; Katsuyuki Fukutake
Journal:  Int J Hematol       Date:  2014-07-27       Impact factor: 2.490

3.  Hereditary Factor X (Stuart-Prower Factor) Deficiency.

Authors:  P K Gupta; H Kumar; S Kumar
Journal:  Med J Armed Forces India       Date:  2011-07-21

4.  Toxicity and recovery in the pregnant mouse after gestational exposure to the cyanobacterial toxin, cylindrospermopsin.

Authors:  N Chernoff; E H Rogers; R D Zehr; M I Gage; D E Malarkey; C A Bradfield; Y Liu; J E Schmid; R H Jaskot; J H Richards; C R Wood; M B Rosen
Journal:  J Appl Toxicol       Date:  2010-10-08       Impact factor: 3.446

5.  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

6.  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

Review 7.  Rare congenital bleeding disorders.

Authors:  Massimo Franchini; Giuseppe Marano; Simonetta Pupella; Stefania Vaglio; Francesca Masiello; Eva Veropalumbo; Vanessa Piccinini; Ilaria Pati; Liviana Catalano; Giancarlo Maria Liumbruno
Journal:  Ann Transl Med       Date:  2018-09

8.  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

9.  Clinical profile of patients with rare inherited coagulation disorders: a retrospective analysis of 67 patients from northern India.

Authors:  Sanjeev Kumar Sharma; Suman Kumar; Tulika Seth; Pravas Mishra; Narendra Agrawal; Gurmeet Singh; Avinash Kumar Singh; Manoranjan Mahapatra; Seema Tyagi; Haraprasad Pati; Renu Saxena
Journal:  Mediterr J Hematol Infect Dis       Date:  2012-10-02       Impact factor: 2.576

10.  Plasma-derived factor X concentrate compassionate use for hereditary factor X deficiency: Long-term safety and efficacy in a retrospective data-collection study.

Authors:  James N Huang; Ri Liesner; Steven K Austin; Kaan Kavakli; Chioma Akanezi
Journal:  Res Pract Thromb Haemost       Date:  2021-07-02
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