Journal of Family Medicine and Primary Care (Jan 2022)

Microspherophakia: A clinical approach and mini review with a case report

  • Sucharita Das,
  • Ajai Agrawal,
  • Prashant K Verma

DOI
https://doi.org/10.4103/jfmpc.jfmpc_1212_22
Journal volume & issue
Vol. 11, no. 12
pp. 7949 – 7952

Abstract

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Microspherophakia refers to a spherophakic lens with a decreased equatorial diameter. Microspherophakia can be found in systemic or ocular conditions, such as Marfan's syndrome, Weill–Marchesani syndrome, iridocorneal endothelial syndrome, and Axenfeld–Rieger syndrome. A 3-year-old girl was brought with complaints of eyes appearing larger, watering and inability to see bright light for 1 year. On examination, she had megalocornea; the cornea was clear with a shallow anterior chamber, and microspherophakic lens. Her intraocular pressure (IOP) was recorded as 43 and 32 mmHg in the right and left eyes, respectively. This article guides in classifying, categorizing, and managing a case with microspherophakia.

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