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[Corneal dystrophies].

S V Trufanov1, L Yu Tekeeva1, E P Salovarova1

  • 1Research Institute of Eye Diseases, 11A Rossolimo St., Moscow, Russian Federation, 119021.

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Summary

This review covers corneal dystrophies, slow-progressing eye conditions, detailing their clinical, morphological, and genetic features. Current treatments focus on symptom management, with surgical options for severe vision loss.

Keywords:
classification of dystrophiescorneacorneal degenerationcorneal dystrophy

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Area of Science:

  • Ophthalmology
  • Genetics
  • Pathology

Background:

  • Corneal dystrophies are a group of slow-progressing, non-inflammatory corneal pathologies.
  • These conditions often exhibit variable associated traits, necessitating careful differential diagnosis from acute inflammatory eye diseases.
  • Accurate diagnosis is crucial as dystrophies require different management than urgent inflammatory conditions.

Purpose of the Study:

  • To review the modern clinical, morphological, and genetic aspects of corneal dystrophies.
  • To provide an overview based on the latest international classification (2015).
  • To highlight the importance of differential diagnosis and current treatment strategies.

Main Methods:

  • Review of recent international classification of corneal dystrophies.
  • Analysis of clinical, morphological, and genetic data.
  • Synthesis of information on diagnostic and therapeutic approaches.

Main Results:

  • Corneal dystrophies are characterized by slow progression and non-inflammatory nature.
  • Differential diagnosis from acute inflammatory conditions is critical.
  • Current conservative treatments are symptomatic (lubricants, epithelizing agents, contact lenses).
  • No targeted etiological treatments are currently available.

Conclusions:

  • Effective management of corneal dystrophies relies on accurate diagnosis and symptomatic treatment.
  • Surgical interventions like phototherapeutic keratectomy and keratoplasty are options for vision-impairing cases.
  • Further research into targeted etiopathogenetic treatments is warranted.