Response to spectral-domain optical coherence tomography foveal morphology as a prognostic factor for vision performance in congenital aniridia. [PDF]
Eur J Ophthalmol, 2022 Rufai SR, Thomas MG, Gottlob I.
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Reciprocal effects of conditioned medium on gene and protein expression of limbal epithelial cells and limbal fibroblasts in congenital aniridia. [PDF]
PLoS OneBerger M +9 more
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Coexistence of Congenital Aniridia and Ptosis in a Patient with Neurofibromatosis Type I: A Case Report. [PDF]
Case Rep OphthalmolMancini M +5 more
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Intraocular use of methotrexate (MTX) for the treatment of proliferative vitreoretinopathy (PVR) in congenital aniridia (CI) and a possible link to aniridia fibrosis syndrome (AFS) treatment. [PDF]
Am J Ophthalmol Case RepAmbati NR, Riemann CD.
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Familial occurrence of congenital aniridia
Klinika Oczna, 1992 <p>Aniridia and coloboma iridis are congenital defects which are inherited in common as an autosomal dominant trait. The study presents an analysis of 15 pedigrees of 15 patients from 3 families; it confirms the hereditary character of aniridia and iris coloboma and indicates the variability of the genetic expression.</p>
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A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region. [PDF]
BMC Med Genomics, 2020 Vasilyeva TA +14 more
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Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome. [PDF]
Genes (Basel), 2020 Vasilyeva TA +4 more
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Management of Congenital Aniridia-Associated Keratopathy: Long-Term Outcomes from a Tertiary Referral Center. [PDF]
Am J Ophthalmol, 2020 Yazdanpanah G +11 more
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