Search results for "Familial exudative vitreoretinopathy"

showing 1 items of 1 documents

Total retinal detachment caused by a KIF11 mutation.

2017

Purpose This is a case report of bilateral retinal detachment associated with KIF11 mutation. Methods In our university hospital, an 8-week-old patient presented with a potential bilateral congenital cataract, iris atrophy, and iridocorneal contact in the left eye. An examination revealed microcephaly and edema of the dorsa of the feet. The eye examination showed a clear lens in both eyes with a dislodged anterior chamber in the left eye with vessels drawn from the iris to the lens. A retrolental white bilateral mass with vessels was also observed. The MRI and the ultrasound revealed a potential peritoneal hyperplastic glass body. Bilateral retinal detachment was diagnosed during surgery. R…

Microcephalymedicine.medical_specialtyDNA Mutational AnalysisKinesinsRetina03 medical and health sciences0302 clinical medicineOphthalmologyDNA Mutational AnalysismedicineTotal retinal detachmentHumans030219 obstetrics & reproductive medicinemedicine.diagnostic_testbusiness.industryInfant NewbornRetinal DetachmentRetinal detachmentMagnetic resonance imagingGeneral Medicinemedicine.diseaseUniversity hospitalMagnetic Resonance ImagingOphthalmologyMutation (genetic algorithm)Mutation030221 ophthalmology & optometryFamilial exudative vitreoretinopathybusinessEuropean journal of ophthalmology
researchProduct