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mastoiditis/reductase
Veza se sprema u međuspremnik
3 rezultati
Lemierre's syndrome with double heterozygote status in the methylenetetrahydrofolate reductase gene.
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BACKGROUND
There are some risk factors being more vulnerable to Lemierre's syndrome such as a hypercoagulable state.
METHODS
We report a rare case of Lemierre's syndrome with ethmoid and maxillary sinusitis, bilateral mastoiditis, and sigmoid sinus thrombosis.
RESULTS
Genetic study revealed a double
Inherited prothrombotic risk factors and cerebral venous thrombosis.
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Fifteen patients with cerebral venous thrombosis were ascertained retrospectively. Their case notes were reviewed, and stored or new blood was assayed for factor V Leiden (FVL) mutation, prothrombin gene mutation 20201A, and 5,10 methylene tetrahydrofolate reductase (MTHFR) C677T mutation. A
Recurrent thromboembolism in infants and children suffering from symptomatic neonatal arterial stroke: a prospective follow-up study.
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OBJECTIVE
The present study was performed to evaluate the rate of recurrent symptomatic thromboembolism with respect to prothrombotic risk factors and underlying clinical conditions.
METHODS
In a series of 215 consecutively enrolled neonates with arterial ischemic stroke (AIS), the factor V G1691A
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