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An ROP screening dilemma: hereditary cataracts developing in a premature infant after birth
Inna Marcus1, Daniel J Salchow, Kathleen M Stoessel
1Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, CT, USA.
Insights
Early cataract removal in premature infants is crucial for timely retinopathy of prematurity (ROP) screening. This case highlights the necessity of prompt intervention to ensure adequate visual assessment in high-risk neonates.
Area of Science:
- Ophthalmology
- Neonatology
- Genetics
Background:
- Premature infants face unique ocular challenges, including retinopathy of prematurity (ROP).
- Hereditary cataracts can complicate ROP screening in neonates.
- Timely ROP evaluation is critical for preventing vision loss in premature infants.
Abstract:
A female infant born prematurely at 23 weeks' gestational age developed bilateral hereditary cataracts at post-menstrual age 33 weeks, which precluded retinopathy of prematurity screening. The infant underwent right cataract extraction 1 week later, and retinopathy of prematurity was monitored by examining the right eye. In the seventeenth week of life (post-menstrual age 40 weeks), the cataract was removed from the left eye. Visual outcome at 19 months of age was good in both eyes. Very early cataract extraction may be necessary in premature infants to allow ROP evaluations.
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