Results 131 to 140 of about 2,109 (161)
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Teratogenically induced congenital aphakia
Experimental Eye Research, 1964Forty-five offspring of pregnant DBA mice treated with a single large dose of vitamin A were serially sectioned. Nearly all of the young had bilateral “typical” retinal coloboma with otherwise well-developed eyes. One of them, however, had more severe abnormalities, consisting of a microphthalmic left eye and an extensively malformed right one, in ...
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P20.12: Prenatal diagnosis of congenital aphakia
Ultrasound in Obstetrics & Gynecology, 2010Multigravida A.P., 37 years old, was referred at 32 weeks of gestation to tertiary ultrasound unit because of BPD adequate for 38 gestational weeks. At the detailed scan absence of the right lens was diagnosed (images a, b), borderline ventriculomegaly and macrocephaly. The rest of morphology was normal.
A. Novakov Mikic +4 more
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Primary congenital aphakia and the rubella syndrome
Teratology, 1975AbstractFour embryos from women infected by rubella virus early in pregnancy were investigated histologically. In three of the patients the serological tests were positive; in the fourth the diagnosis of rubella was based solely on the clinical picture. Three of the four embryos showed unilateral severe microphthalmia and primary congenital aphakia. In
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Corneal Perforation With Secondary Congenital Aphakia in Peters Anomaly
Cornea, 2005To describe two cases of secondary congenital aphakia in association with Peters anomaly.Two infants were noted to have corneal opacification at birth. Each child was found to have Peters anomaly requiring corneal transplantation in 1 or both eyes.Each child underwent penetrating keratoplasty, revealing absence of the crystalline lens in 1 eye ...
Chris S, Banning +3 more
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Lack of FOXE3 coding mutation in a case of congenital aphakia
Ophthalmic Genetics, 2017To report the findings in a patient with congenital primary aphakia, a rare disease known to be caused by mutations in the FOXE3 gene.The clinical appearances and visual functions of the patient were determined from the medical records. Genetic analyses were performed to search for mutations in the FOXE3 gene by Sanger sequencing and whole exome ...
Yusuke Sano +4 more
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Use of Anterior Segment OCT in the Evaluation and Management of Congenital Aphakia
Journal of Pediatric Ophthalmology & Strabismus, 2010Anterior segment optical coherence tomography (AS-OCT) is a noninvasive technology capable of capturing high-resolution images of the anterior segment. With AS-OCT, a 7-year-old boy with nystagmus was diagnosed as having secondary congenital aphakia. The presence of lens capsules on the AS-OCT was of significant prognostic and management value and the ...
Vanissa W S, Chow +2 more
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Peter's anomaly with congenital aphakia.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 1980An Inuit boy was born with microphthalmia and a central corneal opacity of the right globe. Histopathologic examination revealed a central adherent corneal leukoma (Peter's anomaly) as well as absence of the lens. We are not aware of other well documented histopathologic reports of congenital aphakia and Peter's anomaly occurring in the same eye.
R, Harris, S, Brownstein, J M, Little
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Unilateral Primary Congenital Aphakia
American Journal of Ophthalmology, 1964J R, WOLTER, R C, HALL, G L, MASON
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[Aphakia correction with rigid contact lenses in congenital cataract].
Journal francais d'ophtalmologie, 2013To describe follow-up and evaluate functional results of rigid gas-permeable contact lens wear for the correction of aphakia in infants after surgery for congenital cataract.This retrospective study was performed on 23 eyes of 17 children (12 boys and five girls), between three days and 36 months of age (median 3.5 months), undergoing cataract ...
C, Loudot +3 more
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