In:
Pathophysiology of Haemostasis and Thrombosis, S. Karger AG, Vol. 36, No. 2 ( 2007), p. 102-104
Abstract:
Here we report a case of Hirschsprung’s disease presenting with acute complete splenic infarction due to thrombus in the splenic vena. MTHFR C677T (methylenetetrahydrofolate) gene homozygote mutation was a risk factor for thrombosis. According to our knowledge, this is the first report for a Hirschsprung’s disease patient with acute complete splenic infarct due to isolated splenic vein thrombosis accompanied by MTHFR C677T gene homozygote mutation.
Type of Medium:
Online Resource
ISSN:
1424-8832
,
1424-8840
Language:
English
Publisher:
S. Karger AG
Publication Date:
2007
detail.hit.zdb_id:
2081182-2
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