"Factor VII Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.
| Descriptor ID |
D005168
|
| MeSH Number(s) |
C15.378.100.100.310 C15.378.100.141.310 C15.378.463.310 C16.320.099.310
|
| Concept/Terms |
Factor VII Deficiency- Factor VII Deficiency
- Deficiency, Factor Seven
- Deficiencies, Factor Seven
- Factor Seven Deficiencies
- Factor Seven Deficiency
- Hypoproconvertinemia
- Hypoproconvertinemias
- Deficiency, Factor VII
- Deficiencies, Factor VII
- Factor VII Deficiencies
- Deficiency, Factor 7
- Deficiencies, Factor 7
- Factor 7 Deficiencies
- Factor 7 Deficiency
|
Below are MeSH descriptors whose meaning is more general than "Factor VII Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Factor VII Deficiency".
This graph shows the total number of publications written about "Factor VII Deficiency" by people in this website by year, and whether "Factor VII Deficiency" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Factor VII Deficiency" by people in Profiles.
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Yoon U, Haley S, Huffnagle S, Huffnagle J. Viscoelastic testing guided coagulation management in factor VII deficiency for spinal anaesthesia and caesarean section. BMJ Case Rep. 2024 Jun 19; 17(6).
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Yeom RS, Wang XA, Elia E, Yoon U. Severe Congenital Factor VII Deficiency with Normal Perioperative Coagulation Profile Based on ROTEM Analysis in a Hepatectomy. Am J Case Rep. 2021 Aug 10; 22:e930245.
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Jenkins TL, Zheng CX, Murchison AP, Bilyk JR. Orbital Compartment Syndrome Following Post-Traumatic Subgaleal Hematoma. Ophthalmic Plast Reconstr Surg. 2017 Mar/Apr; 33(2):e33-e36.
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Rajpurkar M, Callaghan M, Frey MJ, Set K, Chugani H, Sood S. Management of intracranial surgery for refractory epilepsy in severe factor VII deficiency: choosing the optimal dosing regimen. Haemophilia. 2014 May; 20(3):e234-7.
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Peyvandi F, De Cristofaro R, Garagiola I, Palla R, Akhavan S, Landolfi R, Mannucci PM. The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency. Br J Haematol. 2004 Dec; 127(5):576-84.
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Peyvandi F, De Cristofaro R, Akhavan S, Carew JA, Landolfi R, Bauer KA, Mannucci PM. Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity. Thromb Haemost. 2002 Nov; 88(5):750-5.
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Slease RB, Schumacher HR. Deficiency of coagulation factors VII and XII in a patient with Hodgkin's disease. Arch Intern Med. 1977 Nov; 137(11):1633-5.