Difference between revisions of "Lynch syndrome"

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[[Image:Tumour-infiltrating lymphocytes - 2 -- very high mag.jpg|thumb|right|[[Micrograph]] showing [[tumour infiltrating lymphocytes]], a finding seen in Lynch syndrome.]]

[[Image:Tumour-infiltrating lymphocytes - 2 -- very high mag.jpg|thumb|right|250px||[[Micrograph]] showing [[tumour infiltrating lymphocytes]], a finding seen in Lynch syndrome.]]

'''Lynch syndrome''', also '''hereditary non-polyposis colorectal cancer syndrome''' (abbreviated '''HNPCC'''), is a constellation of clinical findings caused by a mutation in a mismatch repair gene, of which there are several.<ref name=OMIM120435>{{OMIM|120435}}</ref>

Difference between revisions of "Lynch syndrome"

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Revision as of 05:19, 12 August 2014 (view source) Michael (talk \| contribs) ← Older edit		Revision as of 05:52, 12 August 2014 (view source) Michael (talk \| contribs) Newer edit →
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	[[Image:Tumour-infiltrating lymphocytes - 2 -- very high mag.jpg\|thumb\|right\|[[Micrograph]] showing [[tumour infiltrating lymphocytes]], a finding seen in Lynch syndrome.]]		[[Image:Tumour-infiltrating lymphocytes - 2 -- very high mag.jpg\|thumb\|right\|250px\|\|[[Micrograph]] showing [[tumour infiltrating lymphocytes]], a finding seen in Lynch syndrome.]]
	'''Lynch syndrome''', also '''hereditary non-polyposis colorectal cancer syndrome''' (abbreviated '''HNPCC'''), is a constellation of clinical findings caused by a mutation in a mismatch repair gene, of which there are several.<ref name=OMIM120435>{{OMIM\|120435}}</ref>		'''Lynch syndrome''', also '''hereditary non-polyposis colorectal cancer syndrome''' (abbreviated '''HNPCC'''), is a constellation of clinical findings caused by a mutation in a mismatch repair gene, of which there are several.<ref name=OMIM120435>{{OMIM\|120435}}</ref>