The prothrombin G20210A mutation is a risk factor for sudden hearing loss in young patients

Thrombosis and Haemostasis

Volumn 86, Issue 4, 2001, Pages 1118-1119

  Patscheke, J H ^a   Arndt, J ^a   Dietz, K ^a   Zenner, H P ^a   Reuner, K H ^a  

^a ZLMT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

3' UNTRANSLATED REGION; ADULT; AGED; ARTERY THROMBOSIS; BLOOD CLOTTING; CASE CONTROL STUDY; CONTROLLED STUDY; FEMALE; GENE MUTATION; HETEROZYGOSITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; PATHOPHYSIOLOGY; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; STATISTICAL ANALYSIS; SUDDEN DEAFNESS; THROMBOCYTE ACTIVATION; THROMBOEMBOLISM; VEIN THROMBOSIS;

EID: 0034764880     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1616544     Document Type: Letter

References (11)

1. Non-functioning posterior communicating arteries of circle of Willis in idiopathic sudden hearing loss
2. Hypotension and sensorineural hearing loss: A possible correlation
3. Blood viscosity and plasma viscosity in patients with sudden deafness
4. Sudden sensorineural hearing loss: A viral etiology?
5. Anti-endothelial autoantibodies in patients with sudden hearing loss
6. Effects of experimental cochlear thrombosis on oxygenation and auditory function of the inner ear
7. Thrombophilia
8. Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
9. The 20210A allele of the prothrombin gene is an independent risk factor for perception deafness in patients with venous thromboembolic antecedents
10. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis