| Literature DB >> 22033913 |
S Schönland1, N Blank, A V Kristen, J Beimler, T Ganten, U Hegenbart.
Abstract
Amyloidoses are rare protein folding disorders, in which proteins are deposited as insoluble fibrillar aggregates due to a conformational change. This can occur in a local or systemic form. Systemic amyloidoses are life-threatening complications of monoclonal gammopathy, chronic inflammatory diseases or within hereditary diseases. The causative treatment of amyloidosis is the reduction of the amyloid precursor protein by chemotherapy, anti-inflammatory treatment, or liver transplantation. Early diagnosis of the disease is essential in order to effectively treat patients and avoid further deterioration of organ functions.Entities:
Mesh:
Year: 2012 PMID: 22033913 DOI: 10.1007/s00108-011-2952-y
Source DB: PubMed Journal: Internist (Berl) ISSN: 0020-9554 Impact factor: 0.743