Finnish type amyloidosis
From Wikipedia, the free encyclopedia
| Finnish type amyloidosis Classification and external resources |
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| ICD-9 | 277.3 |
|---|---|
| OMIM | 105120 |
| DiseasesDB | 32688 |
Finnish type amyloidosis is a form of amyloidosis associated with gelsolin.[1]
[edit] Presentation
Associated conditions include cutis laxa[2] and ataxia.[3]
[edit] References
- ^ de la Chapelle A, Kere J, Sack GH, Tolvanen R, Maury CP (July 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.
- ^ Kiuru-Enari S, Keski-Oja J, Haltia M (February 2005). "Cutis laxa in hereditary gelsolin amyloidosis". Br. J. Dermatol. 152 (2): 250–7. doi:. PMID 15727635.
- ^ Tanskanen M, Paetau A, Salonen O, et al (March 2007). "Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report". Amyloid 14 (1): 89–95. doi:. PMID 17453628.
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