Korean J Ophthalmol > Volume 19(2); 2005 > Article
Korean Journal of Ophthalmology 2005;19(2):112-115.
DOI: https://doi.org/10.3341/kjo.2005.19.2.112    Published online June 30, 2005.
Bilateral Retinal Dysplasia and Secondary Glaucoma Associated with Homozygous Protein C Deficiency.
Un Chul Park, Ho Kyung Choung, Seong Joon Kim, Young Suk Yu
1Department of Ophthalmology, Seoul National University Children's Hospital, Seoul, Korea. ysyu@snu.ac.kr
2Department of Ophthalmology, Seoul National University Boramae Hospital, Seoul, Korea.
3Seoul Artificial Eye Center, Seoul National University Hospital Clinical Research Institute, Seoul, Korea.
Protein C deficiency is an autosomal recessive disorder, which predisposes the patient to potentially blinding and widespread lethal thromboembolic complications, especially in the homozygous type. We here report the first Korean case of ophthalmic involvement and its surgical treatment in homozygous protein C deficiency. METHODS: A 3.4kg, full term girl was born by normal delivery but showed bilateral leukocoria on day 2. Laboratory results disclosed a very low protein C activity level (10%) in the patient and moderately decreased levels in the other family members. Ophthalmic examination showed bilateral corneal opacity and shallow anterior chamber. B-scan ultrasonography which showed intravitreal mass lesions without microphthalmos and a funnel-shaped retinal detachment suggested bilateral retinal dysplasia. RESULTS: As the eyes were under progression of secondary glaucoma, bilateral lensectomies were performed at 2 months old and corneal opacity was regressed to some degree. However, at 14 months old, the left eye showed moderate corneal opacity with a band keratopathy. CONCLUSIONS: Although visual outcome was very poor after surgery, we could impede or slow down the progression of secondary glaucoma and save the eyeballs in the infant with homozygous protein C deficiency.
Key Words: Corneal opacity;Homozygous protein C deficiency;Retinal dysplasia;Secondary glaucoma

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