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| {{Infobox_Disease |
| | #REDIRECT [[Gelosline related amyloidosis]] |
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| DiseasesDB = 32688 |
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| ICD9 = {{ICD9|277.3}} |
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| OMIM = 105120 |
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| {{SI}}
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| '''Finnish type amyloidosis''' is a form of [[amyloidosis]] associated with [[gelsolin]].<ref name="pmid1322359">{{cite journal |author=de la Chapelle A, Kere J, Sack GH, Tolvanen R, Maury CP |title=Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family |journal=Genomics |volume=13 |issue=3 |pages=898–901 |year=1992 |month=July |pmid=1322359 |doi= |url=http://linkinghub.elsevier.com/retrieve/pii/0888-7543(92)90182-R}}</ref>
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| ==Presentation==
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| Associated conditions include [[cutis laxa]]<ref name="pmid15727635">{{cite journal |author=Kiuru-Enari S, Keski-Oja J, Haltia M |title=Cutis laxa in hereditary gelsolin amyloidosis |journal=Br. J. Dermatol. |volume=152 |issue=2 |pages=250–7 |year=2005 |month=February |pmid=15727635 |doi=10.1111/j.1365-2133.2004.06276.x |url=http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=0007-0963&date=2005&volume=152&issue=2&spage=250}}</ref> and [[ataxia]].<ref name="pmid17453628">{{cite journal |author=Tanskanen M, Paetau A, Salonen O, ''et al'' |title=Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report |journal=Amyloid |volume=14 |issue=1 |pages=89–95 |year=2007 |month=March |pmid=17453628 |doi=10.1080/13506120601116393 |url=http://www.informaworld.com/openurl?genre=article&doi=10.1080/13506120601116393&magic=pubmed||1B69BA326FFE69C3F0A8F227DF8201D0}}</ref>
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| ==References==
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| {{reflist|2}}
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| {{Amyloidosis}}
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| {{Nephrology}}
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| [[Category:Metabolic disorders]]
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