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abstract: Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature. We report a case of 7 years old male child who presented to us as a diagnosed case of factor 7 deficiency with recurrent epistaxis.
altloc:
  - http://www.ojhas.org/issue36/2010-4-17.htm
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creators_id:
  - gsnarang321@gmail.com
  - ~
  - ~
creators_name:
  - family: Narang
    given: Gursharan Singh
    honourific: ''
    lineage: ''
  - family: Arora
    given: Sunita
    honourific: ''
    lineage: ''
  - family: Pahwa
    given: Jivtesh Singh
    honourific: ''
    lineage: ''
date: 2011-01-20
date_type: published
datestamp: 2011-05-02 17:16:43
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dir: disk0/00/00/72/60
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editors_id:
  - BS Kakkilaya
editors_name:
  - family: Kakkilaya
    given: Srinivas
    honourific: Dr
    lineage: ''
eprint_status: archive
eprintid: 7260
fileinfo: /style/images/fileicons/application_pdf.png;/7260/1/2010%2D4%2D17.pdf
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keywords: Combined factor VII and X deficiency
lastmod: 2011-05-02 17:16:43
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number: 4
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pubdom: TRUE
publication: Online Journal of Health and Allied Sciences
publisher: BS Kakkilaya
refereed: TRUE
referencetext: "1.\tPeyvandi F, Mannucci PM. Rare coagulation disorders. Thromb Haemost 1999;82(4):1207-1214.\r\n2.\tUprichard J, Perry DJ. Factor X deficiency. Blood Rev 2002;16(2):97-110.\r\n3.\tRoberts HR, Escobar MA. Inherited disorders of prothrombin conversion, In: Colman RW, Marder VJ, Clowes AW, Geroge JN, Goldhaber SZ, eds. Hemostasis and thrombosis – Basic principles and clinical practice. 5th edition. Philadelphia: Lippincott Williams & Wilkins, 2006; 923-37.\r\n4.\tGirolami A, Scandellari R, Scapin M, Vettore S. Congenital bleeding disorder of the vitamin K-dependent clotting factors. Vitram Horm 2008;78:281-374.    \r\n5.\tMannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood 2004;104:1243-1252.\r\n6.\tGirolami A, Ruzzon E, Tezza F, Scandellari R, Scapin M, Scarparo P Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature. Haemophilia 2008;14(2):323-328.\r\n7.\tBoxus G, Slacmeudler M, Ninane J. Combined hereditary deficiency in factors VII and X revealed by a prolonged partial thromboplastin time. Arch Pediatr 1997;4(1):44-47.\r\n8.\tGupta PK, Kumar H, Kumar S. Hereditary Factor X (Stuart-Power Factor) Deficiency. MJAFI 2008;64:286-287.\r\n9.\tKinra P, Kumar H. Recombinant Factor VIIA. MJAFI 2009;65:59-61\r\n10.\tFranchini M. Recombinant Factor VIIa: A Review on its Clincal use. International Journal of Hematology. 2006;83(2):126-138."
relation_type: []
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reportno: ~
rev_number: 18
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status_changed: 2011-05-02 17:16:43
subjects:
  - OJHAS
succeeds: ~
suggestions: ~
sword_depositor: ~
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thesistype: ~
title: Combined Factor VII and X Deficiency
type: journale
userid: 4338
volume: 9
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