Literature DB >> 27213768

The Genetics and Pathophysiology of IC3D Category 1 Corneal Dystrophies: A Review.

Verity Frances Oliver1, Andrea Louise Vincent.   

Abstract

Corneal dystrophies are a group of inherited disorders affecting the cornea, many of which lead to visual impairment. The International Committee for Classification of Corneal Dystrophies has established criteria to clarify the status of the various corneal dystrophies, which include the knowledge of the underlying genetics. In this review, we discuss the International Committee for Classification of Corneal Dystrophies category 1 (second edition) corneal dystrophies, for which a clear genetic link has been established. We highlight the various mechanisms underlying corneal dystrophy pathology, including structural disorganization, instability or maladhesion, aberrant protein stability and deposition, abnormal cellular proliferation or apoptosis, and dysfunction of normal enzymatic processes. Understanding these genetic mechanisms is essential for designing targets for therapeutic intervention, especially in the age of gene therapy and gene editing.

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Year:  2016        PMID: 27213768     DOI: 10.1097/APO.0000000000000205

Source DB:  PubMed          Journal:  Asia Pac J Ophthalmol (Phila)        ISSN: 2162-0989


  2 in total

1.  Delivery of Antisense Oligonucleotides to the Cornea.

Authors:  Viet Q Chau; Jiaxin Hu; Xin Gong; John D Hulleman; Rafael L Ufret-Vincenty; Frank Rigo; Thahza P Prakash; David R Corey; V Vinod Mootha
Journal:  Nucleic Acid Ther       Date:  2020-03-23       Impact factor: 5.486

2.  Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy.

Authors:  Giuseppe Acri; Antonio Micali; Rosalia D'Angelo; Domenico Puzzolo; Pasquale Aragona; Barbara Testagrossa; Emanuela Aragona; Edward Wylegala; Anna Nowinska
Journal:  J Clin Med       Date:  2022-03-04       Impact factor: 4.241

  2 in total

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