Literature DB >> 21416382

Posterior microphthalmos pigmentary retinopathy syndrome.

Niranjan Pehere1, Subhadra Jalali, Himanshu Deshmukh, Chitra Kannabiran.   

Abstract

Posterior Microphthalmos Pigmentary Retinopathy Syndrome (PMPRS). Posterior microphthalmos (PM) is a relatively infrequent type of microphthalmos where posterior segment is predominantly affected with normal anterior segment measurements. Herein, we report two siblings with posterior microphthalmos retinopathy syndrome with postulated autosomal recessive mode of inheritance. A 13-year-old child had PM and retinitis pigmentosa (RP) and his 7-year-old sister had PM, RP, and foveoschisis. The genetics of this syndrome and variable phenotype is discussed. Importance of being aware of posterior microphthalmos and its posterior segment associations is highlighted.

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Year:  2011        PMID: 21416382     DOI: 10.1007/s10633-011-9266-1

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  11 in total

1.  ISCEV Standard for full-field clinical electroretinography (2008 update).

Authors:  M F Marmor; A B Fulton; G E Holder; Y Miyake; M Brigell; M Bach
Journal:  Doc Ophthalmol       Date:  2008-11-22       Impact factor: 2.379

2.  A novel mutation confirms MFRP as the gene causing the syndrome of nanophthalmos-renititis pigmentosa-foveoschisis-optic disk drusen.

Authors:  Jaume Crespí; José A Buil; Francisca Bassaganyas; José I Vela-Segarra; Jesús Díaz-Cascajosa; Raul Ayala-Ramírez; Juan C Zenteno
Journal:  Am J Ophthalmol       Date:  2008-06-13       Impact factor: 5.258

3.  Hereditary posterior microphthalmos with papillomacular fold and high hyperopia.

Authors:  M Spitznas; E Gerke; J B Bateman
Journal:  Arch Ophthalmol       Date:  1983-03

4.  Relative anterior microphthalmos: morphometric analysis and its implications for cataract surgery.

Authors:  G U Auffarth; M Blum; U Faller; M R Tetz; H E Völcker
Journal:  Ophthalmology       Date:  2000-08       Impact factor: 12.079

5.  Posterior segment changes associated with posterior microphthalmos.

Authors:  Moncef Khairallah; Riadh Messaoud; Sonia Zaouali; Selim Ben Yahia; Ahmed Ladjimi; Salah Jenzri
Journal:  Ophthalmology       Date:  2002-03       Impact factor: 12.079

6.  A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation.

Authors:  Raul Ayala-Ramirez; Federico Graue-Wiechers; Violeta Robredo; Monica Amato-Almanza; Iliana Horta-Diez; Juan Carlos Zenteno
Journal:  Mol Vis       Date:  2006-12-04       Impact factor: 2.367

7.  A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.

Authors:  Rajarshi Mukhopadhyay; Panagiotis I Sergouniotis; Donna S Mackay; Alexander C Day; Genevieve Wright; Sophie Devery; Bart P Leroy; Anthony G Robson; Graham E Holder; Zheng Li; Andrew R Webster
Journal:  Mol Vis       Date:  2010-03-26       Impact factor: 2.367

8.  Aetiology of severe visual impairment and blindness in microphthalmos.

Authors:  M J Elder
Journal:  Br J Ophthalmol       Date:  1994-05       Impact factor: 4.638

9.  Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia.

Authors:  Annaïck Desmaison; Adeline Vigouroux; Claudine Rieubland; Christine Peres; Patrick Calvas; Nicolas Chassaing
Journal:  Mol Vis       Date:  2010-12-18       Impact factor: 2.367

10.  Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex.

Authors:  Juan Carlos Zenteno; Beatriz Buentello-Volante; Miguel A Quiroz-González; Miguel A Quiroz-Reyes
Journal:  Mol Vis       Date:  2009-09-05       Impact factor: 2.367

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  5 in total

1.  High-hyperopia database, part I: clinical characterisation including morphometric (biometric) differentiation of posterior microphthalmos from nanophthalmos.

Authors:  N Relhan; S Jalali; N Pehre; H L Rao; U Manusani; L Bodduluri
Journal:  Eye (Lond)       Date:  2015-10-23       Impact factor: 3.775

2.  Report on ocular biometry of microphthalmos, retinal dystrophy, flash electroretinography, ocular coherence tomography, genetic analysis and the surgical challenge of entropion correction in a rare case of Hallermann-Streiff-Francois syndrome.

Authors:  Deepa Jagadish Muthugaduru; Chinmaya Sahu; Mohammad Javed Ali; Ashwin Dalal; Subhadra Jalali
Journal:  Doc Ophthalmol       Date:  2013-06-01       Impact factor: 2.379

3.  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

4.  Membrane frizzled-related protein gene-related ophthalmological syndrome: 30-month follow-up of a sporadic case and review of genotype-phenotype correlation in the literature.

Authors:  Alberto Neri; Rosachiara Leaci; Juan C Zenteno; Cristina Casubolo; Elisabetta Delfini; Claudio Macaluso
Journal:  Mol Vis       Date:  2012-10-26       Impact factor: 2.367

5.  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

  5 in total

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