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Pathological Myopia

Also known as: Degenerative Myopia, Myopic Maculopathy

High myopia with structural changes of the posterior segment from progressive axial elongation of the globe, typically axial length above 26 mm and a spherical equivalent worse than -6.00 dioptres, with degenerative fundus complications that can cause irreversible visual loss. It is a leading cause of blindness in East Asia and is rising worldwide.

  • Prevalence of high myopia in young adults: 5 to 20 percent in urban East Asia, 2 to 5 percent elsewhere.
  • Risk factors: early onset of myopia, parental myopia, prolonged near work, little outdoor time, female sex, and genetic and syndromic causes (Stickler, Marfan, Ehlers-Danlos, retinopathy of prematurity, congenital stationary night blindness).
  • Complications:
    • Posterior staphyloma, lacquer cracks, chorioretinal atrophy (myopic maculopathy, graded from tessellated fundus to patchy and macular atrophy).
    • Myopic choroidal neovascularisation (about 5 to 10 percent), with a Fuchs spot (pigmented scar).
    • Myopic traction maculopathy (foveoschisis, macular detachment, lamellar and full-thickness macular hole).
    • Retinal tears and rhegmatogenous detachment (lifetime risk about 5 percent above -6 dioptres), lattice degeneration, and giant tear.
    • Glaucoma (2 to 3 times risk), early cataract, and tilted optic disc with peripapillary atrophy and myopic optic neuropathy.

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