ALECT2 amyloidosis
MONDO:0018588A rare, systemic amyloidosis characterized by slowly progressive renal disease presenting with proteinuria, hypertension and decreased glomerular filtration rate leading to progressive renal failure. Histology reveals amyloid deposits of leukocyte chemotactic factor-2 protein in the renal cortical interstitium, tubular basement membranes, glomeruli and the vessel walls. Extra-renal deposits can be seen in the liver, lungs, spleen and adrenal glands.
Also known as: LECT2 amyloidosis, leukocyte chemotactic factor-2 amyloidosis
3 clinical trials for this condition and its sub-types, 0 tagged with ALECT2 amyloidosis itself.
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