Literature DB >> 299986

Unusual superficial variant of granular dystrophy of the cornea.

R Haddad, R L Font, B S Fine.   

Abstract

Two patients with a superficial variant of granular dystrophy of the cornea occurring primarily in nongrafted eyes developed rapid progression of clinical manifestations and visual deterioration at an early age. No other members of their family were known to be affected. A clinical diagnosis of superficial corneal dystrophy, type undetermined, was made. The histopathologic features of the corneas resembled the findings seen in Reis-Bücklers dystrophy and led to some confusion in the differential diagnosis. Electron microscopic studies in both cases unequivocally established the diagnosis of granular dystrophy.

Entities:  

Mesh:

Year:  1977        PMID: 299986     DOI: 10.1016/0002-9394(77)90619-5

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  10 in total

1.  [Corneal dystrophies and molecular genetics. Results of current research reveal prospects for new therapeutic possibilities].

Authors:  H Witschel
Journal:  Ophthalmologe       Date:  2002-06       Impact factor: 1.059

2.  Homogeneity of kerato-epithelin codon 124 mutations in Japanese patients with either of two types of corneal stromal dystrophy.

Authors:  Y Mashima; Y Imamura; M Konishi; A Nagasawa; M Yamada; Y Oguchi; J Kudoh; N Shimizu
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

3.  Alcohol epitheliectomy with mechanical debridement in a case of granular corneal dystrophy with r555w homozygous mutation of TGF B1 gene.

Authors:  Prashant Garg; Aneeta Jabbar
Journal:  Indian J Ophthalmol       Date:  2010 Jul-Aug       Impact factor: 1.848

4.  Bilateral recurrence of granular corneal dystrophy in the grafts. A clinico-pathologic study.

Authors:  H Witschel; R Sundmacher
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1979-01-15

5.  Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients.

Authors:  Xiao-Dan Hao; Yang-Yang Zhang; Peng Chen; Su-Xia Li; Ye Wang
Journal:  Int J Ophthalmol       Date:  2016-02-18       Impact factor: 1.779

6.  Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients.

Authors:  Y Mashima; M Konishi; Y Nakamura; Y Imamura; M Yamada; T Ogata; J Kudoh; N Shimizu
Journal:  Br J Ophthalmol       Date:  1998-11       Impact factor: 4.638

Review 7.  The IC3D classification of the corneal dystrophies.

Authors:  Jayne S Weiss; H U Møller; Walter Lisch; Shigeru Kinoshita; Anthony J Aldave; Michael W Belin; Tero Kivelä; Massimo Busin; Francis L Munier; Berthold Seitz; John Sutphin; Cecilie Bredrup; Mark J Mannis; Christopher J Rapuano; Gabriel Van Rij; Eung Kweon Kim; Gordon K Klintworth
Journal:  Cornea       Date:  2008-12       Impact factor: 2.651

8.  TGFBI gene mutations in a Korean population with corneal dystrophy.

Authors:  Kyong Jin Cho; Jee Won Mok; Kyung Sun Na; Chang Rae Rho; Yong Soo Byun; Ho Sik Hwang; Kyu Yeon Hwang; Choun-Ki Joo
Journal:  Mol Vis       Date:  2012-07-20       Impact factor: 2.367

9.  Phenotype-genotype correlations in patients with TGFBI-linked corneal dystrophies in Taiwan.

Authors:  Yu-Chih Hou; I-Jong Wang; Cheng-Hsiang Hsiao; Wei-Li Chen; Fung-Rong Hu
Journal:  Mol Vis       Date:  2012-02-07       Impact factor: 2.367

Review 10.  Corneal dystrophies.

Authors:  Gordon K Klintworth
Journal:  Orphanet J Rare Dis       Date:  2009-02-23       Impact factor: 4.123

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.