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February 5, 2026Indian Journal of Ophthalmology - Case Reports0 citations

Striking case of Weil–Marchesani syndrome with an extremely thick cornea

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SSSwati ShokeenSGShalini GuptaSTSwati Tomar

Key Points

  • To discuss a unique case of Weil–Marchesani syndrome featuring significant corneal thickness and high myopia.
  • Patient presentation of symptoms and clinical measurements
  • Slit-lamp and gonioscopy examinations
  • Cataract surgery with iris claw implantation
  • Best corrected visual acuities were 6/24 and 6/60
  • Corneal thicknesses were recorded at 711 and 734 microns
  • Intraocular pressures were 28 and 32 mmHg
  • Surgery revealed less than normal lens equatorial diameter
  • Zonular weakness necessitated iris claw implantation

Abstract

A 41-year-old male presented with diminution of vision in both eyes since the past 3 months. He was a high myope with a refractive error of -16D and -19D, best corrected visual acuities of 6/24 and 6/60, intraocular pressures measured with Goldmann applanation tonometry of 28 and 32 mmHg, and central corneal thicknesses of 711 and 734 microns in the right and left eyes, respectively. The patient had short stature and brachydactyly. Slit-lamp examination revealed clear cornea, irregular anterior chamber depth, and immature cataract in both eyes. Gonioscopy showed open angles in both eyes. On dilated anterior segment examination, lens equator could be appreciated super-temporally in the right eye and superiorly in the left eye. Fundus examination was normal except for tortuous blood vessels. He was diagnosed as a case of Weil Marchesani syndrome and was advised cataract surgery. Peroperatively, the equatorial diameter of the lens was appreciated to be less than normal. The patient underwent cataract removal with iris claw implantation due to severe zonular weakness.

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Cite This Study

Shokeen et al. (2026) studied this question.

synapsesocial.com/papers/698434a6f1d9ada3c1fb2fdchttps://doi.org/10.4103/ijo.ijo_1181_25
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