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Pathophysiology and Histopathology of Keratoconus

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Keratoconus

Abstract

From the widely held concept of keratoconus being a bilateral noninflammatory corneal disorder, more insights into its pathophysiology have led us to understand about this disease being multifactorial in origin. The origins of the disease are determined only partly by genetic factors, and it appears to have a complex pathogenesis. The progression and association have been noted with environmental stimuli and coexisting ocular disease such as allergy and several systemic conditions. Histopathologically, changes are noted in all layers of the cornea; however, the hallmark of this condition is stromal thinning. An interplay between proteinase enzymes leading to their upregulation and downregulation of proteinase inhibitors leads to biomechanical corneal instability. Early changes do not affect the vision, and some patients have mild disease with slow or no progression. In others, there appears to be a precipitous progression leading to extremely poor vision if left untreated. In this chapter, we describe the potential pathophysiological mechanisms in keratoconus and discuss in detail the histopathological changes.

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Acknowledgments

  1. 1.

    Dr. Vijayalakshmi Idimadakala for editing help.

  2. 2.

    Mr. Chenchu Naidu and Mr. B Sreedhar for histopathology slides.

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Hyderabad Eye Research Foundation, Hyderabad, India.

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Correspondence to Somasheila I. Murthy .

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Murthy, S.I., Mishra, D.K., Rathi, V.M. (2022). Pathophysiology and Histopathology of Keratoconus. In: Das, S. (eds) Keratoconus. Springer, Singapore. https://doi.org/10.1007/978-981-19-4262-4_4

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  • DOI: https://doi.org/10.1007/978-981-19-4262-4_4

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