Amyloidosis pathophysiology: Difference between revisions
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Replaced content with "__NOTOC__ {{Amyloidosis}} {{CMG}}; {{AE}} {{SHH}} ==Overview== ==Pathophysiology== ===Systemic Amyloidosis=== ====Primary/Hereditary Amyloidosis==== ====Secondary Am..." |
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* Amyloid is an abnormal extracellular fibrillar protein that deposit in the tissues and causes disturbance of organ function and a wide variety of clinical syndromes that are classified according to the respective fibril protein precursor.<ref name="pmid23979488">{{cite journal |vauthors=Gillmore JD, Hawkins PN |title=Pathophysiology and treatment of systemic amyloidosis |journal=Nat Rev Nephrol |volume=9 |issue=10 |pages=574–86 |date=October 2013 |pmid=23979488 |doi=10.1038/nrneph.2013.171 |url=}}</ref> | |||
* In systemic amyloidosis, amyloid deposition is widespread and amyloid typically accumulate gradually. | |||
====Primary/Hereditary Amyloidosis==== | ====Primary/Hereditary Amyloidosis==== | ||
Revision as of 14:52, 3 May 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]
Overview
Pathophysiology
Systemic Amyloidosis
- Amyloid is an abnormal extracellular fibrillar protein that deposit in the tissues and causes disturbance of organ function and a wide variety of clinical syndromes that are classified according to the respective fibril protein precursor.[1]
- In systemic amyloidosis, amyloid deposition is widespread and amyloid typically accumulate gradually.
Primary/Hereditary Amyloidosis
Secondary Amyloidosis
Organ-specific Amyloidosis
Gross Pathology
Microscopic Pathology
Other Diseases Associated with the Amyloid Protein
Serum Amyloid P Component
References
- ↑ Gillmore JD, Hawkins PN (October 2013). "Pathophysiology and treatment of systemic amyloidosis". Nat Rev Nephrol. 9 (10): 574–86. doi:10.1038/nrneph.2013.171. PMID 23979488.