Amyloidosis V

Amyloidosis V

*Gene map locus 9q34

Amyloid cranial neuropathy with lattice corneal dystrophy

Amyloidosis due to mutant gelsolin

Corneal dystrophy, lattice type II

Finnish type amyloidosis

Lattice corneal dystrophy, type II

Meretoja type amyloidosis

[Clinical features: corneal lattice dystrophy; cranial neuropathy]

[Inheritance: autosomal dominant]


Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family	Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family	Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family
British Journal of Ophthalmology	British Journal of Ophthalmology	British Journal of Ophthalmology


Corneal Morphology and Sensitivity in Lattice Dystrophy Type II (Familial Amyloidosis, Finnish Type)	Corneal Morphology and Sensitivity in Lattice Dystrophy Type II (Familial Amyloidosis, Finnish Type)	Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East
Investigative Ophthalmology & Visual Science	Investigative Ophthalmology & Visual Science	Nephrology Dialysis Transplantation


Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East
Nephrology Dialysis Transplantation

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Edited by Aldo Campana, August 21, 2012