Neurotrophic keratopathy (NK) is a degenerative rare disease characterized by a reduced or absent corneal sensitivity and an impairment of corneal nerves [1]. The trophism and transparency of the cornea, which lacks blood and lymphatic vessels, is mainly due to its extensive innervation from the ophthalmic branch of the trigeminal nerve [2]. Any trauma, infection, surgery, systemic, or local congenital diseases may damage corneal nerves and cause neurotrophic keratopathy (NK). Impairment or loss of corneal sensory innervation is responsible for corneal epithelial defects, ulcer, and perforation. The epidemiology of NK is still uncertain. As a rare disease, its estimated prevalence is less than 30/100,000 individuals [3].

Neurotrophic keratopathy / Surico, Pier Luigi; De Gregorio, Chiara; Mori, Tommaso; Di Zazzo, Antonio. - (2025), pp. 61-68. [10.1007/978-981-96-0495-1_5].

Neurotrophic keratopathy

Surico, Pier Luigi
Primo
;
2025

Abstract

Neurotrophic keratopathy (NK) is a degenerative rare disease characterized by a reduced or absent corneal sensitivity and an impairment of corneal nerves [1]. The trophism and transparency of the cornea, which lacks blood and lymphatic vessels, is mainly due to its extensive innervation from the ophthalmic branch of the trigeminal nerve [2]. Any trauma, infection, surgery, systemic, or local congenital diseases may damage corneal nerves and cause neurotrophic keratopathy (NK). Impairment or loss of corneal sensory innervation is responsible for corneal epithelial defects, ulcer, and perforation. The epidemiology of NK is still uncertain. As a rare disease, its estimated prevalence is less than 30/100,000 individuals [3].
2025
Cornea Casebook
9789819604944
9789819604951
neurotrophic keratitis; cornea; ulcer
02 Pubblicazione su volume::02a Capitolo o Articolo
Neurotrophic keratopathy / Surico, Pier Luigi; De Gregorio, Chiara; Mori, Tommaso; Di Zazzo, Antonio. - (2025), pp. 61-68. [10.1007/978-981-96-0495-1_5].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1736432
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