Literature DB >> 12543751

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.

M A Reddy1, P J Francis, V Berry, K Bradshaw, R J Patel, E R Maher, R Kumar, S S Bhattacharya, A T Moore.   

Abstract

AIM: To phenotype and genetically map the disease locus in a family presenting with autosomal dominant microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.
METHODS: Six affected and three unaffected members of the pedigree were examined. All individuals provided a history and underwent a full clinical examination with A-scan and B-scan ultrasonography and electrophysiological testing where appropriate. PCR based microsatellite marker genotyping using a positional candidate gene approach was then performed on DNA samples extracted from venous blood provided by each subject.
RESULTS: The disorder is inherited as an autosomal dominant trait with variable expressivity and has a complex phenotype. Affected individuals had bilateral microcornea, pulverulent-like lens opacities, a rod-cone dystrophy and posterior staphyloma (MRCS). Using a positional candidate gene approach, the authors have evidence suggestive of linkage of this disorder to a region on 11q13 within the nanophthalmos 1 (NNO1) genetic interval. The small family size militates against achieving a LOD score of 3, but the haplotype data and the position of the putative MRCS locus within a known nanophthalmos locus are suggestive of linkage. A candidate gene within this region (ROM1) was screened and no mutations were found in affected members of the family.
CONCLUSION: This rare developmental disorder has some phenotypic similarities to nanophthalmos and possibly maps to a locus within the genetic interval encompassing the NNO1 locus. Screening of candidate genes within this region continues.

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Year:  2003        PMID: 12543751      PMCID: PMC1771505          DOI: 10.1136/bjo.87.2.197

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  35 in total

1.  Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.

Authors:  V Berry; P Francis; S Kaushal; A Moore; S Bhattacharya
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

2.  Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.

Authors:  E Ferda Percin; L A Ploder; J J Yu; K Arici; D J Horsford; A Rutherford; B Bapat; D W Cox; A M Duncan; V I Kalnins; A Kocak-Altintas; J C Sowden; E Traboulsi; M Sarfarazi; R R McInnes
Journal:  Nat Genet       Date:  2000-08       Impact factor: 38.330

3.  Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.

Authors:  N Azuma; A Hirakiyama; T Inoue; A Asaka; M Yamada
Journal:  Hum Mol Genet       Date:  2000-02-12       Impact factor: 6.150

4.  [The microphthalmia-retinitis pigmentosa-glaucoma syndrome].

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Journal:  Arch Ophtalmol Rev Gen Ophtalmol       Date:  1958 Jan-Feb

5.  Connexin46 mutations in autosomal dominant congenital cataract.

Authors:  D Mackay; A Ionides; Z Kibar; G Rouleau; V Berry; A Moore; A Shiels; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

6.  Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.

Authors:  E V Semina; I Brownell; H A Mintz-Hittner; J C Murray; M Jamrich
Journal:  Hum Mol Genet       Date:  2001-02-01       Impact factor: 6.150

7.  Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.

Authors:  K Kajiwara; E L Berson; T P Dryja
Journal:  Science       Date:  1994-06-10       Impact factor: 47.728

8.  Retinitis pigmentosa, nanophthalmos, and optic disc drusen: a case report.

Authors:  Y M Buys; C J Pavlin
Journal:  Ophthalmology       Date:  1999-03       Impact factor: 12.079

9.  A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

Authors:  L Morlé; M Bozon; J C Zech; N Alloisio; A Raas-Rothschild; C Philippe; J C Lambert; J Godet; H Plauchu; P Edery
Journal:  Am J Hum Genet       Date:  2000-10-13       Impact factor: 11.025

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  9 in total

Review 1.  Bestrophin 1 and retinal disease.

Authors:  Adiv A Johnson; Karina E Guziewicz; C Justin Lee; Ravi C Kalathur; Jose S Pulido; Lihua Y Marmorstein; Alan D Marmorstein
Journal:  Prog Retin Eye Res       Date:  2017-01-30       Impact factor: 21.198

2.  Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT.

Authors:  Caterina Toma; Giulio Ruberto; Federico Marzi; Giulio Vandelli; Sabrina Signorini; Enza Maria Valente; Mauro Antonini; Chiara Bertone; Paolo Emilio Bianchi
Journal:  Doc Ophthalmol       Date:  2018-07-10       Impact factor: 2.379

3.  Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations.

Authors:  A C Cohn; C Turnbull; J B Ruddle; R H Guymer; L S Kearns; S Staffieri; H T Daggett; A W Hewitt; D A Mackey
Journal:  Eye (Lond)       Date:  2010-11-26       Impact factor: 3.775

4.  An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.

Authors:  Li-Yun Zhang; Gary Hin-Fai Yam; Pancy Oi-Sin Tam; Ricky Yiu-Kwong Lai; Dennis Shun-Chiu Lam; Chi-Pui Pang; Dorothy Shu-Ping Fan
Journal:  Mol Vis       Date:  2009-06-04       Impact factor: 2.367

5.  Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.

Authors:  Sancy Low; Alice E Davidson; Graham E Holder; Chris R Hogg; Shomi S Bhattacharya; Graeme C Black; Paul J Foster; Andrew R Webster
Journal:  Mol Vis       Date:  2011-08-23       Impact factor: 2.367

6.  Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.

Authors:  C Crowley; R Paterson; T Lamey; T McLaren; J De Roach; E Chelva; J Khan
Journal:  Doc Ophthalmol       Date:  2014-05-24       Impact factor: 2.379

7.  Variable expressivity of BEST1-associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree.

Authors:  Mariana Matioli da Palma; Maurício E Vargas; Amanda Burr; Rui Chen; Mark E Pennesi; Richard G Weleber; Paul Yang
Journal:  BMJ Open Ophthalmol       Date:  2021-10-21

8.  Screening for BEST1 gene mutations in Chinese patients with bestrophinopathy.

Authors:  Rong Tian; Guoxing Yang; Jing Wang; Youxin Chen
Journal:  Mol Vis       Date:  2014-11-11       Impact factor: 2.367

9.  Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorder.

Authors:  Yoshiro Morimoto; Mihoko Shimada-Sugimoto; Takeshi Otowa; Shintaro Yoshida; Akira Kinoshita; Hiroyuki Mishima; Naohiro Yamaguchi; Takatoshi Mori; Akira Imamura; Hiroki Ozawa; Naohiro Kurotaki; Christiane Ziegler; Katharina Domschke; Jürgen Deckert; Tadashi Umekage; Mamoru Tochigi; Hisanobu Kaiya; Yuji Okazaki; Katsushi Tokunaga; Tsukasa Sasaki; Koh-Ichiro Yoshiura; Shinji Ono
Journal:  Transl Psychiatry       Date:  2018-02-02       Impact factor: 6.222

  9 in total

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