家族性腎澱粉樣變

家族性腎澱粉樣變
(Familial renal amyloidosis)
家族性腎澱粉樣變; (Familial renal amyloidosis)
類型	腎病、澱粉樣變、rare genetic renal disease[]、secondary glomerular disease[]、Heredofamilial amyloidosis[]、amyloid nephropathy[]、疾病
分類和外部資源
醫學專科	內分泌學
ICD-10	E85.0
ICD-9-CM	277.3
OMIM	105200
DiseasesDB	33335
eMedicine	med/3379
Orphanet	85450
	[編輯此條目的維基數據]

家族性腎澱粉樣變(Familial renal amyloidosis、或稱"家族性內臟澱粉樣變性病"(familial visceral amyloidosis)，或"遺傳性澱粉樣腎病"(hereditary amyloid nephropathy)）爲原發性呈現在腎的一種澱粉樣變形式。^[1]

Quick Facts 家族性腎澱粉樣變 (Familial renal amyloidosis), 類型 ...

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變樣延伸

它與纖維蛋白原α鏈(Fibrinogen alpha chain)、^[2] 載脂蛋白，^[3] 及溶菌酶相關聯。^[4]^[5]

它也被稱為"奧斯特塔格型"(Ostertag)，名稱來自"B·奧斯特塔格"(B. Ostertag)，奧斯特塔格在1932年和1950年以間對"家族性腎澱粉樣變"病症特點提出描述。^[6]^[7]

註釋

[1]
Amyloid. （原始內容存檔於2019-02-17）.
[2]
Uemichi T, Liepnieks JJ, Gertz MA, Benson MD. Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis. Amyloid. September 1998, 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.
[3]
Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715 . PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始內容存檔於2019-09-25）.
[4]
Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始內容存檔於2019-09-25）.
[5]
Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始內容存檔於2012-02-15）.
[6]
Ostertag B. Demonstration einer eigenartigen familiaren paraamyloidose. Zentralbl Aug Pathol. 1932, 56: 253–4.
[7]
Ostertag, B. Familiaere Amyloid-erkrankung. Z. Menschl. Vererb. Konstitutionsl. 1950, 30: 105–115.

[urlAmyloid-1] [1]
Amyloid. （原始內容存檔於2019-02-17）.

[pmid9818055-2] [2]
Uemichi T, Liepnieks JJ, Gertz MA, Benson MD. Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis. Amyloid. September 1998, 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.

[pmid1502149-3] [3]
Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715 . PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始內容存檔於2019-09-25）.

[pmid15745733-4] [4]
Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始內容存檔於2019-09-25）.

[pmid16523055-5] [5]
Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始內容存檔於2012-02-15）.

[6] [6]
Ostertag B. Demonstration einer eigenartigen familiaren paraamyloidose. Zentralbl Aug Pathol. 1932, 56: 253–4.

[7] [7]
Ostertag, B. Familiaere Amyloid-erkrankung. Z. Menschl. Vererb. Konstitutionsl. 1950, 30: 105–115.

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