TNOA Journal of Ophthalmic Science and Research (Jan 2020)

Ocular manifestations of homocystinuria due to cystathionine beta-synthase deficiency: A rare case report with genetic analysis

  • Damaris Magdalene,
  • Ronel Soibam,
  • Riddhi Raichura,
  • Saurabh Deshmukh,
  • Surpriya Hawaibam,
  • Krati Gupta

DOI
https://doi.org/10.4103/tjosr.tjosr_86_20
Journal volume & issue
Vol. 58, no. 4
pp. 302 – 303

Abstract

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Microspherophakia is a developmental lens anomaly characterized by increased anteroposterior diameter and reduced equatorial diameter, which predisposes to secondary glaucoma. A 12-year-old boy presented with diminution of vision. Slit-lamp examination showed anteriorly dislocated crystalline lens. Blood analysis revealed elevated homocysteine levels. Genetic analysis showed cystathionine beta-synthase gene mutation, thus confirming the diagnosis of homocystinuria. To prevent secondary glaucoma, the patient was taken up for surgical intervention. This report highlights a case of homocystinuria with microspherophakia diagnosed with the help of genetic testing.

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