Finnish type amyloidosis
Finnish type amyloidosis | |
ICD-9 | 277.3 |
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OMIM | 105120 |
DiseasesDB | 32688 |
Finnish type amyloidosis is a form of amyloidosis associated with gelsolin.[1]
Presentation
Associated conditions include cutis laxa[2] and ataxia.[3]
References
- ↑ de la Chapelle A, Kere J, Sack GH, Tolvanen R, Maury CP (1992). "Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family". Genomics. 13 (3): 898–901. PMID 1322359. Unknown parameter
|month=
ignored (help) - ↑ Kiuru-Enari S, Keski-Oja J, Haltia M (2005). "Cutis laxa in hereditary gelsolin amyloidosis". Br. J. Dermatol. 152 (2): 250–7. doi:10.1111/j.1365-2133.2004.06276.x. PMID 15727635. Unknown parameter
|month=
ignored (help) - ↑ Tanskanen M, Paetau A, Salonen O; et al. (2007). "Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report". Amyloid. 14 (1): 89–95. doi:10.1080/13506120601116393. PMID 17453628. Text "1B69BA326FFE69C3F0A8F227DF8201D0" ignored (help); Unknown parameter
|month=
ignored (help)
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