ALECT2 amyloidosis

MONDO:0018588

A 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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Amyloidosis (322)

Including sub-types (3) Tagged with ALECT2 amyloidosis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.