Familial renal amyloidosis
| Familial renal amyloidosis | |
|---|---|
| Specialty | Endocrinology  |
Familial renal amyloidosis (or familial visceral amyloidosis, or hereditary amyloid nephropathy) is a form of amyloidosis primarily presenting in the kidney.[1]
It is associated with fibrinogen alpha chain,[2] apolipoprotein A1,[3] and lysozyme.[4][5]
It is also known as "Ostertag" type, after B. Ostertag, who characterized it in 1932 and 1950.[6][7]
References
- ^ "Amyloid".
- ^ Uemichi T, Liepnieks JJ, Gertz MA, Benson MD (September 1998). "Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis". Amyloid. 5 (3): 188–92. doi:10.3109/13506129809003844. PMID 9818055.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Soutar AK; Hawkins PN; Vigushin DM; et al. (August 1992). "Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis". Proc. Natl. Acad. Sci. U.S.A. 89 (16): 7389–93. doi:10.1073/pnas.89.16.7389. PMC 49715. PMID 1502149.
{{cite journal}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ Granel B; Serratrice J; Disdier P; et al. (March 2005). "Underdiagnosed amyloidosis: amyloidosis of lysozyme variant". Am. J. Med. 118 (3): 321–2. doi:10.1016/j.amjmed.2004.10.022. PMID 15745733.
{{cite journal}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ Granel B; Valleix S; Serratrice J; et al. (January 2006). "Lysozyme amyloidosis: report of 4 cases and a review of the literature". Medicine (Baltimore). 85 (1): 66–73. doi:10.1097/01.md.0000200467.51816.6d. PMID 16523055.
{{cite journal}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ Ostertag B. (1932). "Demonstration einer eigenartigen familiaren paraamyloidose". Zentralbl Aug Pathol. 56: 253–4.
- ^ Ostertag, B. (1950). "Familiaere Amyloid-erkrankung". Z. Menschl. Vererb. Konstitutionsl. 30: 105–115.
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