Search articles, concepts, and chapters
4 articles in GJC
OCT confirmed superior optic disc defects and reduced retinal nerve fiber layer thickness in superior segmental optic hypoplasia (SSOH). This provides a quantitative tool for diagnosing subtle SSOH previously undetected.
Kakiuchi-Matsumoto T, Isashiki Y, Ohba N, Kimura K, Sonoda S, Unoki K
This study found a novel CYP1B1 gene mutation (R444Q) in Japanese primary congenital glaucoma patients, suggesting about 20% of cases may be genetic, impacting diagnosis and understanding disease variability.
Kakiuchi T, Isashiki Y, Nakao K, Sonoda S, Kimura K, Ohba N
A novel CYP1B1 gene mutation was found in a Japanese patient with primary infantile glaucoma, confirming worldwide genetic links but suggesting ethnic prevalence differences for this severe childhood glaucoma.
A 2-month-old's lens hemorrhage in congenital cataract was likely caused by a ruptured hyaloid artery, highlighting a rare etiology for this condition.
All 4 articles loaded