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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 3
1969 5
1970 5
1971 3
1972 4
1973 2
1974 8
1975 5
1976 2
1977 7
1978 2
1979 6
1980 7
1981 5
1982 5
1983 7
1984 3
1985 4
1986 4
1987 1
1988 3
1989 5
1990 4
1991 5
1992 9
1993 6
1994 6
1995 12
1996 15
1997 20
1998 15
1999 18
2000 12
2001 18
2002 10
2003 15
2004 14
2005 19
2006 26
2007 31
2008 20
2009 15
2010 24
2011 40
2012 28
2013 19
2014 30
2015 27
2016 31
2017 31
2018 49
2019 55
2020 37
2021 34
2022 31
2023 10
2024 5

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757 results

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Quoted phrase not found in phrase index: "Abnormal anterior eye segment morphology"
Page 1
The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature.
Meuwissen ME, Halley DJ, Smit LS, Lequin MH, Cobben JM, de Coo R, van Harssel J, Sallevelt S, Woldringh G, van der Knaap MS, de Vries LS, Mancini GM. Meuwissen ME, et al. Genet Med. 2015 Nov;17(11):843-53. doi: 10.1038/gim.2014.210. Epub 2015 Feb 26. Genet Med. 2015. PMID: 25719457 Free article. Review.
COL4A1 and COL4A2 mutations have been reported with a broader spectrum of cerebrovascular, renal, ophthalmological, cardiac, and muscular abnormalities, indicated as "COL4A1 mutation-related disorders." Genetic counseling is challenging because of broad phenotypic variatio …
COL4A1 and COL4A2 mutations have been reported with a broader spectrum of cerebrovascular, renal, ophthalmological, cardiac, and muscular …
Normal and abnormal foveal development.
Thomas MG, Papageorgiou E, Kuht HJ, Gottlob I. Thomas MG, et al. Br J Ophthalmol. 2022 May;106(5):593-599. doi: 10.1136/bjophthalmol-2020-316348. Epub 2020 Nov 4. Br J Ophthalmol. 2022. PMID: 33148537 Review.
This is a characteristic feature for example in albinism, aniridia, prematurity, foveal hypoplasia with optic nerve decussation defects with or without anterior segment dysgenesis without albinism (FHONDA) and optic nerve hypoplasia. ...In preverbal children grading …
This is a characteristic feature for example in albinism, aniridia, prematurity, foveal hypoplasia with optic nerve decussation defects with …
Biomarkers in the Occurrence and Development of Pterygium.
He S, Wu Z. He S, et al. Ophthalmic Res. 2022;65(5):481-492. doi: 10.1159/000523878. Epub 2022 Apr 11. Ophthalmic Res. 2022. PMID: 35405677 Free article. Review.
The pathogenesis of pterygium is complex, and various biomarkers provide new targets for treatment and prognosis. Currently, the most common treatment for pterygium is surgical excision, but it is invasive risk and has a high recurrence rate. ...
The pathogenesis of pterygium is complex, and various biomarkers provide new targets for treatment and prognosis. Currently, the most …
Ocular coloboma.
Pagon RA. Pagon RA. Surv Ophthalmol. 1981 Jan-Feb;25(4):223-36. doi: 10.1016/0039-6257(81)90092-8. Surv Ophthalmol. 1981. PMID: 6782689 Review.
Patients with multiple malformations and coloboma may have a recognized malformation syndrome of unknown etiology, a single gene disorder, or chromosomal abnormality. Prognosis and recurrence risk can be determined only after complete evaluation of the patient and o …
Patients with multiple malformations and coloboma may have a recognized malformation syndrome of unknown etiology, a single gene disorder, o …
Peter's anomaly-A homeotic gene disorder.
Kylat RI. Kylat RI. Acta Paediatr. 2022 May;111(5):948-951. doi: 10.1111/apa.16260. Epub 2022 Jan 31. Acta Paediatr. 2022. PMID: 35044009 Review.
Peter's anomaly is a rare form of congenital anterior segment dysgenesis of the eye. Varying degrees of central corneal opacity and lenticulo-corneal or irido-corneal synechiae are the key hallmarks. ...For the dense leukoma, corneal graft may be neede …
Peter's anomaly is a rare form of congenital anterior segment dysgenesis of the eye. Varying degrees of central …
Pigment dispersion syndrome and pigmentary glaucoma: a review and update.
Scuderi G, Contestabile MT, Scuderi L, Librando A, Fenicia V, Rahimi S. Scuderi G, et al. Int Ophthalmol. 2019 Jul;39(7):1651-1662. doi: 10.1007/s10792-018-0938-7. Epub 2018 May 2. Int Ophthalmol. 2019. PMID: 29721842 Review.
INTRODUCTION: Pigment dispersion syndrome (PDS) is a condition where anomalous iridozonular contact leads to pigment dispersion throughout the anterior segment and the released pigment is abnormally deposited on various ocular structures. ...Typical alteratio …
INTRODUCTION: Pigment dispersion syndrome (PDS) is a condition where anomalous iridozonular contact leads to pigment dispersion throughout t …
Ocular manifestations in classic homocystinuria.
Gus PI, Donis KC, Marinho D, Martins TF, de Souza CFM, Carloto RB, Leivas G, Schwartz IVD. Gus PI, et al. Ophthalmic Genet. 2021 Feb;42(1):71-74. doi: 10.1080/13816810.2020.1821384. Epub 2020 Sep 17. Ophthalmic Genet. 2021. PMID: 32940091
Main clinical features may include skeletal and vascular manifestations, developmental delay, intellectual disability and eye disorders. MATERIAL AND METHODS: This is an observational and retrospective study aiming at describing eye abnormalities presented by …
Main clinical features may include skeletal and vascular manifestations, developmental delay, intellectual disability and eye disorde …
Peters Anomaly: Novel Non-Invasive Alternatives to Penetrating Keratoplasty.
Rajagopal RN, Fernandes M. Rajagopal RN, et al. Semin Ophthalmol. 2023 Apr;38(3):275-282. doi: 10.1080/08820538.2023.2176238. Epub 2023 Feb 14. Semin Ophthalmol. 2023. PMID: 36788651 Review.
The relatively recent adoption of high-quality anterior segment imaging in the form of high-frequency ultrasound biomicroscopy and anterior segment optical coherence tomography has aided in the accurate diagnosis of CCOs, facilitated distinction of PA …
The relatively recent adoption of high-quality anterior segment imaging in the form of high-frequency ultrasound biomicroscopy …
Crystalline coloboma.
Demetrio R, Ruiz-Sancho D, Rolón N, del Campo A, Blanco C. Demetrio R, et al. Arch Soc Esp Oftalmol. 2015 Mar;90(3):142-3. doi: 10.1016/j.oftal.2014.02.012. Epub 2014 Nov 15. Arch Soc Esp Oftalmol. 2015. PMID: 25443185 English, Spanish.
CASE REPORT: We present a seventy-three year-old female diagnosed with lens coloboma when she was going to be operated on for cataracts. DISCUSSION: The incidence of congenital coloboma of the eye is estimated to be 0.5 per 10000 newborns in Spain, 1.4 in France, 2. …
CASE REPORT: We present a seventy-three year-old female diagnosed with lens coloboma when she was going to be operated on for cataracts. DIS …
Congenital corneal anesthesia.
Ramaesh K, Stokes J, Henry E, Dutton GN, Dhillon B. Ramaesh K, et al. Surv Ophthalmol. 2007 Jan-Feb;52(1):50-60. doi: 10.1016/j.survophthal.2006.10.004. Surv Ophthalmol. 2007. PMID: 17212990 Review.
Congenital corneal anesthesia is a rare clinical entity that poses a diagnostic dilemma, particularly in the pediatric age group. The sensory deficit may be confined to the cornea, or extend to other divisions of the trigeminal nerve. The sensory deficit may occur as an is …
Congenital corneal anesthesia is a rare clinical entity that poses a diagnostic dilemma, particularly in the pediatric age group. The …
757 results