Results 141 to 150 of about 2,635 (188)

A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature Review. [PDF]

open access: yesGenes (Basel)
Zhao SH   +11 more
europepmc   +1 more source

Anterior segment dysgenesis in Goldenhar syndrome. [PDF]

open access: yesEye (Lond)
Bari A   +5 more
europepmc   +1 more source

Anti-VEGF versus laser photocoagulation for ROP treatment. [PDF]

open access: yesBioinformation
Ukey S   +4 more
europepmc   +1 more source

Colobomatous macrophthalmia with microcornea syndrome: Report of a new pedigree

open access: yesAmerican Journal of Medical Genetics, Part A, 2003
AbstractColobomatous macrophthalmia with microcornea syndrome (MIM 602499) is a very rare eye malformation. To date, only two families with a total number of eight patients have been reported. We report on 13 additional cases in a single three‐generation family and describe the eye findings and quantitative parameters of corneal curvature and axial ...
Ebru Toker, Eda Ozcan, Özlem Yenice
exaly   +5 more sources
Some of the next articles are maybe not open access.

Related searches:

Histology of microcornea complicated by bullous keratopathy

Acta Ophthalmologica, 2001
ABSTRACT. Purpose: To report a child with a microcornea complicated by bullous keratopathy and to present the results of a developmental and histological investigation of a microcornea.Methods: Clinical and histopathological examination.Results: Histopathological examination of the microcornea showed that the microcornea of our case lacked the non ...
Tomoyuki Inoue
exaly   +3 more sources

Home - About - Disclaimer - Privacy