Familial amyloidosis causes: Difference between revisions
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Common causes of familial amyloidosis may include genetic mutations in:<ref name="pmid8464497">{{cite journal |vauthors=Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ |title=Human lysozyme gene mutations cause hereditary systemic amyloidosis |journal=Nature |volume=362 |issue=6420 |pages=553–7 |date=April 1993 |pmid=8464497 |doi=10.1038/362553a0 |url=}}</ref> | Common causes of familial amyloidosis may include genetic mutations in:<ref name="pmid8464497">{{cite journal |vauthors=Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ |title=Human lysozyme gene mutations cause hereditary systemic amyloidosis |journal=Nature |volume=362 |issue=6420 |pages=553–7 |date=April 1993 |pmid=8464497 |doi=10.1038/362553a0 |url=}}</ref> | ||
* | * [[Transthyretin|Transthyretin (TTR)]] | ||
*[[ | * [[Apolipoprotein AI]] | ||
* | * Apolipoprotein AII | ||
* | * [[Fibrinogen A alpha-chain associated amyloidosis|Fibrinogen Aa]] | ||
*[[Lysozyme]] [[ | * [[Lysozyme]] | ||
* | * [[Gelsolin]] | ||
* [[Cystatin C]] | |||
== References == | == References == | ||
Revision as of 15:29, 8 November 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Hereditary amyloidosis can be caused by genetic mutations in different genes including LYZ gene, fibrinogen A alpha polypeptide gene, FGA gene, APOA1 gene, lysozyme gene, and B2M gene.
Causes
Common Causes
Common causes of familial amyloidosis may include genetic mutations in:[1]
- Transthyretin (TTR)
- Apolipoprotein AI
- Apolipoprotein AII
- Fibrinogen Aa
- Lysozyme
- Gelsolin
- Cystatin C
References
- ↑ Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ (April 1993). "Human lysozyme gene mutations cause hereditary systemic amyloidosis". Nature. 362 (6420): 553–7. doi:10.1038/362553a0. PMID 8464497.