» Articles » PMID: 30450315

Clinical Features of Posterior Microphthalmic and Nanophthalmic Eyes

Overview
Specialty Ophthalmology
Date 2018 Nov 20
PMID 30450315
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: To clinically differentiate nanophthalmos (NO) and posterior microphthalmos (PM) and to explore the mechanisms related to papillomacular folds (PMF).

Methods: Medical records of 34 unrelated patients with microphthalmos (54 eyes) from April 2009 to October 2017 were retrospectively reviewed.

Results: Fourteen eyes of 7 unrelated patients with NO and PM were included in the study. The presenting age of the NO cohort was significantly higher compared with the PM cohort (NO: 27±16y; PM: 3.7±0.6y). PMF was more likely to occur in cases with PM than in NO (25% in NO, 100% in PM). The anatomic features of PMF from optical coherence tomography (OCT) included: ganglion cell layer, inner plexiform layer, inner nuclear layer, outer plexiform layer and outer nuclear layer. In eyes without an apparent PMF (these were all NO eyes), rudimentary fovea without a foveal pit was noted. Four eyes that were NO developed angle closure glaucoma. Three NO eyes developed exudative retinal detachment and were successfully treated with lamellar sclerectomy.

Conclusion: Posterior segment changes are pervasive both in PM and NO. Complications like angle closure glaucoma and exudative retinal detachment are likely to occur in eyes with NO but not with PM. Detailed OCT analysis found that PMF was partially a neural retinal issue, suggesting that redundancy of retinal issues involved only inner retinal layers.

Citing Articles

Insight into small eyes: a practical description from phenotypes presentations to the management.

Niazi S, Dhubhghaill S, Doroodgar F, Gatzioufas Z, Dehghan M Int J Ophthalmol. 2024; 17(2):380-391.

PMID: 38371260 PMC: 10827624. DOI: 10.18240/ijo.2024.02.23.


Comparisons of size of foveal avascular zone area among children with posterior microphthalmos, high hyperopia, and normal eyes.

Sasaki K, Sasaki K, Hirota M, Hayashi T, Mizota A Int Ophthalmol. 2022; 42(8):2599-2607.

PMID: 35366136 DOI: 10.1007/s10792-022-02250-4.


Efficacy of fitting HydroCone (Toris K) contact lenses for the visual rehabilitation of patients with posterior microphthalmos.

Karabulut G, Ozcelik F Arq Bras Oftalmol. 2022; 86(4):330-336.

PMID: 35319662 PMC: 11826715. DOI: 10.5935/0004-2749.20230051.


Nanophthalmos: An Update on the Biological Parameters and Fundus Abnormalities.

Yang N, Zhao L, Liu J, Ma L, Zhao J J Ophthalmol. 2021; 2021:8853811.

PMID: 33777447 PMC: 7972840. DOI: 10.1155/2021/8853811.


Posterior segment abnormalities in posterior microphthalmos.

Raval N, Zhang C, Yao W, Lin J Am J Ophthalmol Case Rep. 2020; 20:100915.

PMID: 32964171 PMC: 7490723. DOI: 10.1016/j.ajoc.2020.100915.


References
1.
Ostrin L, Yuzuriha J, Wildsoet C . Refractive error and ocular parameters: comparison of two SD-OCT systems. Optom Vis Sci. 2015; 92(4):437-46. PMC: 4424184. DOI: 10.1097/OPX.0000000000000559. View

2.
Elder M . Aetiology of severe visual impairment and blindness in microphthalmos. Br J Ophthalmol. 1994; 78(5):332-4. PMC: 504780. DOI: 10.1136/bjo.78.5.332. View

3.
Uyama M, Takahashi K, Kozaki J, Tagami N, Takada Y, Ohkuma H . Uveal effusion syndrome: clinical features, surgical treatment, histologic examination of the sclera, and pathophysiology. Ophthalmology. 2000; 107(3):441-9. DOI: 10.1016/s0161-6420(99)00141-4. View

4.
GASS J . Uveal effusion syndrome. A new hypothesis concerning pathogenesis and technique of surgical treatment. Retina. 1983; 3(3):159-63. View

5.
Tekin K, Teke M, Citirik M . CLINICAL APPRAISAL AND RETINAL IMAGING IN POSTERIOR MICROPHTHALMOS. Semin Ophthalmol. 2017; 33(3):412-418. DOI: 10.1080/08820538.2017.1284869. View