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AApoAII amyloidosis

Disease Export to PDF
Name:
AApoAII amyloidosis
Description:
A rare hereditary amyloidosis with primary renal involvement characterized by variable onset of renal insufficiency with edema, hypertension, proteinuria, and azotemia, eventually leading to end-stage renal disease. Amyloid cardiomyopathy and histopathological evidence of amyloid deposition in other organs, such as the spleen, liver, adrenal glands, and pancreas, among others, have also been described.
ORPHAcode:
238269
Synonyms:
Apolipoprotein A-II amyloidosis
Familial amyloid nephropathy due to apolipoprotein A-II variant
Familial renal amyloidosis due to apolipoprotein A-II variant
Hereditary amyloid nephropathy due to apolipoprotein A-II variant
Hereditary renal amyloidosis due to apolipoprotein A-II variant
XREF(s):
Orphanet
ICD-10
Analyte(s):
APOA2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14