1991
DOI: 10.1016/s0002-9394(14)76862-x
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Unilateral Diplophthalmos

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Cited by 8 publications
(2 citation statements)
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“…Congenital biphakia (2 crystalline lenses in the same eye) was first published in a case report by Von Graefe in 1854 2 and is an extremely rare condition, having only been reported in a few cases since. These cases discuss the presence of biphakia with and without other ocular abnormalities, 3 such as hourglass cornea, 1 uveal coloboma, 4 iris coloboma, 2 cleft anterior segment, 5 and diplophthalmos, 6 as well as its appearance alongside congenital na-sal and craniocervical deformities. 4,6 Notably, in our review of the literature on congenital biphakia, all cases presented unilaterally rather than bilaterally.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Congenital biphakia (2 crystalline lenses in the same eye) was first published in a case report by Von Graefe in 1854 2 and is an extremely rare condition, having only been reported in a few cases since. These cases discuss the presence of biphakia with and without other ocular abnormalities, 3 such as hourglass cornea, 1 uveal coloboma, 4 iris coloboma, 2 cleft anterior segment, 5 and diplophthalmos, 6 as well as its appearance alongside congenital na-sal and craniocervical deformities. 4,6 Notably, in our review of the literature on congenital biphakia, all cases presented unilaterally rather than bilaterally.…”
Section: Discussionmentioning
confidence: 99%
“…These cases discuss the presence of biphakia with and without other ocular abnormalities, 3 such as hourglass cornea, 1 uveal coloboma, 4 iris coloboma, 2 cleft anterior segment, 5 and diplophthalmos, 6 as well as its appearance alongside congenital na-sal and craniocervical deformities. 4,6 Notably, in our review of the literature on congenital biphakia, all cases presented unilaterally rather than bilaterally. In the aforementioned report of biphakia with congenital nasal abnormality, the patient also had a bifid eyelid and developmental delay 4 ; by contrast, this patient's developmental abnormalities were limited to right eye biphakia and an orofacial cleft.…”
Section: Discussionmentioning
confidence: 99%