Blood Res.  2017 Sep;52(3):229-231. 10.5045/br.2017.52.3.229.

Combined occurrence of Bernard-Soulier syndrome and prekallikrein deficiency

Affiliations
  • 1Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
  • 2Blood and Cancer Research Center, MAHAK Pediatric Cancer Treatment and Research Center, Tehran, Iran.
  • 3Pediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. h.abolghasemi.ha@gmail.com
  • 4Department of Pediatrics, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Abstract

No abstract available.


MeSH Terms

Bernard-Soulier Syndrome*
Prekallikrein*
Prekallikrein

Reference

1. López JA, Andrews RK, Afshar-Kharghan V, Berndt MC. Bernard-Soulier syndrome. Blood. 1998; 91:4397–4418. PMID: 9616133.
2. Zeerleder S, Asmis L, Redondo M, Sulzer I, Lämmle B. A patient with isolated prolongation of aPTT without hemorrhagic diathesis anamnesis: severe, hereditary factor XII deficiency. Ther Umsch. 1999; 56:509–512. PMID: 10517121.
3. Berndt MC, Shen Y, Dopheide SM, Gardiner EE, Andrews RK. The vascular biology of the glycoprotein Ib-IX-V complex. Thromb Haemost. 2001; 86:178–188. PMID: 11487006.
Article
4. Hoffman R, Benz E, Shattil S, editors. Hematology: Basic principles and practice. 3rd ed. New York, NY: Churchill Livingstone;2000.
5. Pham A, Wang J. Bernard-Soulier syndrome: an inherited platelet disorder. Arch Pathol Lab Med. 2007; 131:1834–1836. PMID: 18081445.
Article
6. Young G, Luban N, White JG. Giant platelet disorders in African-American children misdiagnosed as idiopathic thrombocytopenic purpura. J Pediatr Hematol Oncol. 1999; 21:231–236. PMID: 10363857.
Article
7. Sugi T, Makino T. Factor XII, kininogen and plasma prekallikrein in abnormal pregnancies. Curr Drug Targets. 2005; 6:551–557. PMID: 16026275.
Article
8. George JN, Caen JP, Nurden AT. Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood. 1990; 75:1383–1395. PMID: 2180491.
Article
9. Abolghasemi H, Shahverdi E. Umbilical bleeding: a presenting feature for congenital afibrinogenemia. Blood Coagul Fibrinolysis. 2015; 26:834–835. PMID: 26407137.
10. Toogeh G, Keyhani M, Sharifian R, Safaee R, Emami A, Dalili H. A study of Bernard-Soulier syndrome in Tehran, Iran. Arch Iran Med. 2010; 13:549–551. PMID: 21039013.
11. Dasanu CA, Alexandrescu DT. A case of prekallikrein deficiency resulting in severe recurrent mucosal hemorrhage. AM J Med Sci. 2009; 338:429–430. PMID: 19773642.
Article
12. Schmaier AH, McCrae KR. The plasma kallikrein-kinin system: its evolution from contact activation. J Thromb Haemost. 2007; 5:2323–2329. PMID: 17883591.
Article
13. Sollo DG, Saleem A. Prekallikrein (Fletcher factor) deficiency. Ann Clin Lab Sci. 1985; 15:279–285. PMID: 3849948.
14. Saito H, Goodnough LT, Soria J, Soria C, Aznar J, España F. Heterogeneity of human prekallikrein deficiency (Fletcher trait): evidence that five of 18 cases are positive for cross-reacting material. N Engl J Med. 1981; 305:910–914. PMID: 6792540.
15. François D, Trigui N, Leterreux G, et al. Severe prekallikrein deficiencies due to homozygous C529Y mutations. Blood Coagul Fibrinolysis. 2007; 18:283–286. PMID: 17413767.
Article
Full Text Links
  • BR
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr