Abstract
Objective : To report uncommon eye findings in a case of Soto’s Syndrome. Method: Case report Results : A 10-year-old girl with underlying Soto syndrome under multidisciplinary care presented with a history of bilateral, painless and progressive blurring of vision for 1 year. On examination, she had accelerated linear growth, dysmorphicfacies, macrodolichocephaly, hypertelorism and cognitive impairment. Anterior segment examination revealed bilateral anterior polar cataract and bilateral keratoconus. Conclusion : What this case highlights is that in addition to the classic features of Soto’s syndrome, we found two rare ocular associations in this patient;-_namely, polar cataract and keratoconus. These new additions to the constellation of ocular manifestations of Sotos syndrome serve as a reminder that an ophthalmological evaluation should be a part of the basic workup of children with Sotos syndrome.
Highlights
Soto’s syndrome as first described in 1964 by Soto et al (1965)
What this case highlights is that in addition to the classic features of Soto’s syndrome, we found two rare ocular associations in this patient;-_namely, polar cataract and keratoconus
These new additions to the constellation of ocular manifestations of Sotos syndrome serve as a reminder that an ophthalmological evaluation should be a part of the basic workup of children with Sotos syndrome
Summary
A 10-year-old girl with underlying Soto syndrome under multidisciplinary care presented with a history of bilateral, painless and progressive blurring of vision for 1 year. On examination, she had accelerated linear growth, dysmorphicfacies, macrodolichocephaly, hypertelorism and cognitive impairment. Anterior segment examination revealed bilateral anterior polar cataract and bilateral keratoconus
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