Literature DB >> 314081

Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalized amyloidosis.

P C Donders, L J Blanksma.   

Abstract

The clinical history as well as the general and ophthalmic pathology of a woman with the Meretoja type of hereditary systemic amyloidosis and lattice dystrophy of the cornea is described. Extraocularly, amyloid could be demonstrated in all the arterial walls, the peripheral nerves and in the glomeruli; intraocularly, amyloid was seen in the cornea and the sclera.

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Year:  1979        PMID: 314081     DOI: 10.1159/000308818

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN: 0030-3755            Impact factor:   3.250


  3 in total

1.  Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type.

Authors:  Makiko Taira; Hiroyuki Ishiura; Jun Mitsui; Yuji Takahashi; Toshihiro Hayashi; Jun Shimizu; Takashi Matsukawa; Naoko Saito; Kazumasa Okada; Sadatoshi Tsuji; Hiromasa Sawamura; Shiro Amano; Jun Goto; Shoji Tsuji
Journal:  Neurogenetics       Date:  2012-05-24       Impact factor: 2.660

2.  Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.

Authors:  C Y Gregory; K Evans; S S Bhattacharya
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

3.  Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Authors:  H S Stewart; R Parveen; A E Ridgway; R Bonshek; G C Black
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

  3 in total

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