Literature DB >> 21670352

Posterior microphthalmos as a genetically heterogeneous condition that can be allelic to nanophthalmos.

Mohammed A Aldahmesh, Sawsan R Nowilaty, Fatema Alzahrani, Lama Al-Ebdi, Jawahir Y Mohamed, Mohammed Rajab, Arif O Khan, Fowzan S Alkuraya.   

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Year:  2011        PMID： 21670352     DOI： 10.1001/archophthalmol.2011.129

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  11 in total

1.  Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.

Authors:  Rose Richardson; Jane Sowden; Christina Gerth-Kahlert; Anthony T Moore; Mariya Moosajee
Journal:  Eur J Hum Genet       Date:  2017-01-18       Impact factor: 4.246

2.  Clinical features of posterior microphthalmic and nanophthalmic eyes.

Authors:  Jing-Jing Liu; Yi-Ye Chen; Xiang Zhang; Pei-Quan Zhao
Journal:  Int J Ophthalmol       Date:  2018-11-18       Impact factor: 1.779

3.  Nanophthalmos and hemiretinal vein occlusion: A case report.

Authors:  Ahmad A Albar; Sawsan R Nowilaty; Nicola G Ghazi
Journal:  Saudi J Ophthalmol       Date:  2014-11-27

4.  The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort.

Authors:  Owen M Siggs; Mona S Awadalla; Emmanuelle Souzeau; Sandra E Staffieri; Lisa S Kearns; Kate Laurie; Abraham Kuot; Ayub Qassim; Thomas L Edwards; Michael A Coote; Erica Mancel; Mark J Walland; Joanne Dondey; Anna Galanopoulous; Robert J Casson; Richard A Mills; Daniel G MacArthur; Jonathan B Ruddle; Kathryn P Burdon; Jamie E Craig
Journal:  Clin Genet       Date:  2020-03-05       Impact factor: 4.438

5.  Novel membrane frizzled-related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds.

Authors:  Rosemarie A Wasmann; Jolien S Klein Wassink-Ruiter; Olof H Sundin; Elisa Morales; Joke B G M Verheij; Jan Willem R Pott
Journal:  Acta Ophthalmol       Date:  2013-06-07       Impact factor: 3.761

6.  Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos.

Authors:  Itsuka Matsushita; Hiroyuki Kondo; Akihiko Tawara
Journal:  Jpn J Ophthalmol       Date:  2012-05-09       Impact factor: 2.447

7.  Posterior microphthalmos and papillomacular fold-associated cystic changes misdiagnosed as cystoid macular edema following cataract extraction.

Authors:  Ahmad A Albar; Sawsan R Nowilaty; Nicola G Ghazi
Journal:  Clin Ophthalmol       Date:  2015-01-07

8.  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

9.  The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56.

Authors:  Basamat Almoallem; Gavin Arno; Julie De Zaeytijd; Hannah Verdin; Irina Balikova; Ingele Casteels; Thomy de Ravel; Sarah Hull; Martina Suzani; Anne Destrée; Michelle Peng; Denise Williams; John R Ainsworth; Andrew R Webster; Bart P Leroy; Anthony T Moore; Elfride De Baere
Journal:  Sci Rep       Date:  2020-01-28       Impact factor: 4.379

10.  Acquired retinoschisis resolved after 23Gage pars plana vitrectomy in posterior microphthalmos.

Authors:  Shanshan Yu; Yi Gao; Xiaoling Liang; Yongsheng Huang
Journal:  BMC Ophthalmol       Date:  2014-05-11       Impact factor: 2.209
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