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Literature DB >> 27366696

Characteristics of corneal dystrophies: a review from clinical, histological and genetic perspectives.

Abstract

Corneal dystrophy is a common type of hereditary corneal diseases. It includes many types, which have varied pathology, histology and clinical manifestations. Recently, the examination techniques of ophthalmology and gene sequencing advance greatly, which do benefit to our understanding of these diseases. However, many aspects remain still unknown. And due to the poor knowledge of these diseases, the results of the treatments are not satisfoctory. The purpose of this review was to summarize the clinical, histological and genetic characteristics of different types of corneal dystrophies.

Entities: Disease

Keywords: clinic; corneal dystrophy; gene mutation; histology

Year: 2016 PMID： 27366696 PMCID： PMC4916151 DOI： 10.18240/ijo.2016.06.20

Source DB: PubMed Journal: Int J Ophthalmol ISSN： 2222-3959 Impact factor: 1.779

88 in total

1. Familial occurrence of dot (microcystic), map, fingerprint dystrophy of the cornea.

Authors: P R Laibson; J H Krachmer
Journal: Invest Ophthalmol Date: 1975-05

Review 2. Clinical and basic aspects of gelatinous drop-like corneal dystrophy.

Authors: Satoshi Kawasaki; Shigeru Kinoshita
Journal: Dev Ophthalmol Date: 2011-04-26

3. An immunohistochemical analysis and comparison of posterior polymorphous dystrophy with congenital hereditary endothelial dystrophy.

Authors: Glenn C Cockerham; Nora V Laver; Ahmed A Hidayat; Deborah L McCoy
Journal: Cornea Date: 2002-11 Impact factor: 2.651

4. Disorders of the corneal epithelium. A clinicopathologic study of dot, geographic, and fingerprint patterns.

Authors: M M Rodrigues; B S Fine; P R Laibson; L E Zimmerman
Journal: Arch Ophthalmol Date: 1974-12

5. Posterior polymorphous corneal dystrophy: a disease characterized by epithelial-like endothelial cells which influence management and prognosis.

Authors: J H Krachmer
Journal: Trans Am Ophthalmol Soc Date: 1985

6. Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.

Authors: Vivek S Yellore; M Ali Khan; Nirit Bourla; Sylvia A Rayner; Michael C Chen; Baris Sonmez; Rominder S Momi; Kapil M Sampat; Michael B Gorin; Anthony J Aldave
Journal: Mol Vis Date: 2007-09-24 Impact factor: 2.367

7. A clinical and histopathological study of François-Neetens speckled corneal dystrophy.

Authors: D H Nicholson; W R Green; H E Cross; K R Kenyon; D Massof
Journal: Am J Ophthalmol Date: 1977-04 Impact factor: 5.258

8. Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

Authors: Jacek P Szaflik; Monika Ołdak; Radosław B Maksym; Anna Kamińska; Agnieszka Pollak; Monika Udziela; Rafał Płoski; Jerzy Szaflik
Journal: Mol Vis Date: 2008-09-15 Impact factor: 2.367

9. In vivo laser confocal microscopy findings in patients with map-dot-fingerprint (epithelial basement membrane) dystrophy.

Authors: Akira Kobayashi; Hideaki Yokogawa; Kazuhisa Sugiyama
Journal: Clin Ophthalmol Date: 2012-07-27

10. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.

Authors: Andrew Orr; Marie-Pierre Dubé; Julien Marcadier; Haiyan Jiang; Antonio Federico; Stanley George; Christopher Seamone; David Andrews; Paul Dubord; Simon Holland; Sylvie Provost; Vanessa Mongrain; Susan Evans; Brent Higgins; Sharen Bowman; Duane Guernsey; Mark Samuels
Journal: PLoS One Date: 2007-08-01 Impact factor: 3.240

7 in total

Characteristics of corneal dystrophies: a review from clinical, histological and genetic perspectives.

1. Familial occurrence of dot (microcystic), map, fingerprint dystrophy of the cornea.

Review 2. Clinical and basic aspects of gelatinous drop-like corneal dystrophy.

3. An immunohistochemical analysis and comparison of posterior polymorphous dystrophy with congenital hereditary endothelial dystrophy.

4. Disorders of the corneal epithelium. A clinicopathologic study of dot, geographic, and fingerprint patterns.

5. Posterior polymorphous corneal dystrophy: a disease characterized by epithelial-like endothelial cells which influence management and prognosis.

6. Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.

7. A clinical and histopathological study of François-Neetens speckled corneal dystrophy.

8. Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

9. In vivo laser confocal microscopy findings in patients with map-dot-fingerprint (epithelial basement membrane) dystrophy.

10. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.

1. Automatic segmentation of corneal dystrophy on photographic images based on texture analysis.

2. Multiple excimer laser phototherapeutic keratectomies for Avellino corneal dystrophy: a case report.

3. Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathy.

4. Vps35-deficiency impairs SLC4A11 trafficking and promotes corneal dystrophy.

5. Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan.

Review 6. Corneal dystrophies: pathophysiological, genetic, clinical, and therapeutic considerations.

7. Analysis of TGFBI Gene Mutations in Three Chinese Families with Corneal Dystrophy.