Literature DB >> 18465740

Ultrasound biomicroscopy and OCT findings in posterior microphthalmos.

H Erdol1, M Kola, A Turk, N Akyol.   

Abstract

PURPOSE: Posterior microphthalmos is a rare ocular abnormality. The authors report two siblings with bilateral posterior microphthalmos.
METHODS: Two siblings (aged 10 and 13) were admitted with a history of low degree of vision. Ophthalmologic examinations, ocular ultrasonography, ultrasonic biomicroscopy (UBM), and optical coherence tomography (OCT) investigations were carried out and the results were evaluated. All results were also compared with their normal sibling.
RESULTS: Two siblings with posterior microphthalmos have normal and near normal anterior segment dimensions, shortened axial lengths (smaller than 17 mm), low vision with high hyperopias, papillomacular folds, and crowded optic discs. OCT investigation showed bilateral papillomacular retinal fold and UBM examination showed that ciliary body moved behind the iris towards the pupilla and the iridocorneal angle anomalies in two siblings. These findings were not observed in the normal sibling.
CONCLUSIONS: Posterior microphthalmos can exist in the presence of some ocular anomalies. In this case report, UBM provided new information about the structure of iridocorneal angle and ciliary body.

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Year:  2008        PMID: 18465740     DOI: 10.1177/112067210801800331

Source DB:  PubMed          Journal:  Eur J Ophthalmol        ISSN: 1120-6721            Impact factor:   2.597


  4 in total

1.  Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease.

Authors:  Andreas Gal; Isabella Rau; Leila El Matri; Hans-Jürgen Kreienkamp; Susanne Fehr; Karim Baklouti; Ibtissem Chouchane; Yun Li; Monika Rehbein; Josefine Fuchs; Hans C Fledelius; Kaj Vilhelmsen; Daniel F Schorderet; Francis L Munier; Elsebet Ostergaard; Debra A Thompson; Thomas Rosenberg
Journal:  Am J Hum Genet       Date:  2011-03-11       Impact factor: 11.025

2.  Detailed ophthalmologic evaluation of posterior microphthalmos.

Authors:  Zeynep Alkin; Abdullah Ozkaya; Yalcin Karakucuk; Ahmet Demirok
Journal:  Middle East Afr J Ophthalmol       Date:  2014 Apr-Jun

3.  Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3.

Authors:  Xueshan Xiao; Wenmin Sun; Jiamin Ouyang; Shiqiang Li; Xiaoyun Jia; Zhiqun Tan; J Fielding Hejtmancik; Qingjiong Zhang
Journal:  Hum Genet       Date:  2019-06-06       Impact factor: 4.132

4.  Multimodal imaging in posterior microphthalmos.

Authors:  Reza Karkhaneh; Ahmad Masoumi; Nazanin Ebrahimiadib; Hormoz Chams; Mojtaba Abrishami
Journal:  J Curr Ophthalmol       Date:  2019-02-04
  4 in total

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