Familial renal amyloidosis
From Infogalactic: the planetary knowledge core
Familial renal amyloidosis | |
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Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
ICD-10 | E85.0 |
ICD-9-CM | 277.3 |
OMIM | 105200 |
DiseasesDB | 33335 |
eMedicine | med/3379 |
Patient UK | Familial renal amyloidosis |
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
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