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Thromboembolic diseases
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Thromboembolic diseases

Clinical feature: 

Definition: Hereditary diseases or conditions with increased risk of thromboembolic complications are summarized on this page, which includes venous thrombosis and pulmonary embolism. In rare cases of atrial septal abnormalities, paradoxical embolism may occur, which results in cerebral emboli.

Pathogenesis: Thromboembolic diseases exemplify the interplay of inherited and acquired conditions. Acquired risk factors include advanced age, prolonged immobilization, surgery, fractures, oral contraceptives and other forms of hormone replacement therapy, pregnancy und delivery, malignancies, infectious diseases, and antiphospholipid syndrome. More than half of patients with thromboembolic diseases also possess genetic risk factors. This rate is exceptionally height in cases younger than 45 years and thrombosis at atypical sites. All conditions with increased risk for thromboembolic disease are called thrombophilia or hypercoagulability.

Epidemiology: Among cardiovascular diseases, thromboembolic diseases are the third most common. The incidence is 0,1% per year.

Systematic link table: 

Hereditary vascular disease
Arteriosclerosis
APOB
APOE
HABP2
LDLR
MTHFR
PON1
SLC3A1
Thromboembolic diseases
F2
F5
HABP2
MTHFR
PROC
PROS1
SERPINC1
THBD
VKORC1

Literature: 

Franco RF et al. (2001) Genetic risk factors of venous thrombosis.
Thomas RH et al. (2001) Hypercoagulability syndromes.
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