Literature DB >> 24668238

Lemierre's syndrome with double heterozygote status in the methylenetetrahydrofolate reductase gene.

Mostafa Behpour-Oskooee1, Abdollah Karimi, Shirin Sayyahfar.   

Abstract

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 heterozygote status in the methylenetetrahydrofolate reductase gene including C677T and A1298C.
CONCLUSION: It is suggested to screen patients with Lemierre's syndrome for a hypercoagulable state to consider anticoagulant therapy.

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Year:  2014        PMID: 24668238     DOI: 10.1007/s12519-014-0475-z

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  9 in total

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8.  Cerebral sinovenous thrombosis associated with MTHFR A1298C mutation in the newborn: a case report.

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  9 in total
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  2 in total

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