An autosomal dominant inherited disease of the Gelsolin gene that appears in middle age, marked by fine, spidery branching lines (that form a lattice pattern). It resembles lattice dystrophy type I, except that type II is accompanied by progressive facial palsy and the lesions are more peripheral and less dense.

Also Known As

  • Meretoja Syndrome; Finnish Familial Amyloidosis; Amyloidosis V; Familial Amyloidotic Polyneuropathy IV; Lattice Corneal Dystrophy
  • Gelsolin Type; Systemic Amyloidosis Type V; AGel Amyloidosis