Lattice Corneal Dystrophy Associated with Familial Systemic Amyloidosis (Meretoja's Syndrome)

Author:

Purcell John J.,Rodrigues Merlyn,Chishti M. Ishaq,Riner Ronald N.,Dooley Joseph M.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference16 articles.

1. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms; a previousl;Meretoja;Ann Clin Res,1969

2. Histopathological findings of familial amyloidosis with cranial neuropathy as principle manifestation; report of three cases;Meretoja;Acta Pathol Microbiol Scand [A],1971

3. Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy;Meretoja;Clin Genet,1973

4. Ein hereditares syndrom, bestehend aus peripherer Polyneuropathie, Hautveranderunger und gittriger Dystrophie der Hornhaut;Winkelman;Klin Monatsbl Augenheilkd,1971

5. Lattice dystrophy of the corneal; its connection with preceding episodes of crystals and with subsequent amyloidosis;Kaunisto;Acta Ophthalmol,1973

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