Literature DB >> 11559858

CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservation.

A J Lotery1, A Malik, S A Shami, M Sindhi, B Chohan, C Maqbool, P A Moore, M J Denton, E M Stone.   

Abstract

PURPOSE: To report a new phenotype in retinitis pigmentosa (RP) patients with CRB1 mutations at the RP12 locus. PATIENTS: Thirty-seven patients from two Pakistani families with severe retinitis pigmentosa.
METHODS: Samples were screened with single-strand conformation polymorphism analysis followed by DNA sequencing of the coding sequence of the CRB1 gene.
RESULTS: Two novel CRB1 mutations were discovered. No patients had evidence of preservation of the para-arteriolar retinal pigment epithelium (PPRPE) that has been previously reported in all cases of RP associated with CRB1 mutations.
CONCLUSIONS: Patients with severe autosomal recessive (or simplex) RP who lack the finding of PPRPE should not be excluded from molecular analysis of CRB1 purely because they lack the clinical feature of PPRPE. This report illustrates that RP at the RP12 locus is not clinically uniform. The absence of PPRPE cannot be used to exclude CRB1 as a potential molecular explanation for RP.

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Year:  2001        PMID: 11559858     DOI: 10.1076/opge.22.3.163.2222

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  22 in total

Review 1.  CRB1 mutations in inherited retinal dystrophies.

Authors:  Kinga Bujakowska; Isabelle Audo; Saddek Mohand-Saïd; Marie-Elise Lancelot; Aline Antonio; Aurore Germain; Thierry Léveillard; Mélanie Letexier; Jean-Paul Saraiva; Christine Lonjou; Wassila Carpentier; José-Alain Sahel; Shomi S Bhattacharya; Christina Zeitz
Journal:  Hum Mutat       Date:  2011-12-27       Impact factor: 4.878

Review 2.  Leber congenital amaurosis, from darkness to light: An ode to Irene Maumenee.

Authors:  Razek Georges Coussa; Irma Lopez Solache; Robert K Koenekoop
Journal:  Ophthalmic Genet       Date:  2017-01-17       Impact factor: 1.803

3.  Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxa.

Authors:  Andrew J Lotery; Dominique Baas; Caroline Ridley; Richard P O Jones; Caroline C W Klaver; Edwin Stone; Tomoyuki Nakamura; Andrew Luff; Helen Griffiths; Tao Wang; Arthur A B Bergen; Dorothy Trump
Journal:  Hum Mutat       Date:  2006-06       Impact factor: 4.878

4.  Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype.

Authors:  Stephen H Tsang; Tomas Burke; Maris Oll; Suzanne Yzer; Winston Lee; Yajing Angela Xie; Rando Allikmets
Journal:  Ophthalmology       Date:  2014-05-06       Impact factor: 12.079

5.  Unraveling the genetic complexity of Drosophila stardust during photoreceptor morphogenesis and prevention of light-induced degeneration.

Authors:  Sandra Berger; Natalia A Bulgakova; Ferdi Grawe; Kevin Johnson; Elisabeth Knust
Journal:  Genetics       Date:  2007-07-01       Impact factor: 4.562

6.  Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.

Authors:  Mays Talib; Mary J van Schooneveld; Jan Wijnholds; Maria M van Genderen; Nicoline E Schalij-Delfos; Herman E Talsma; Ralph J Florijn; Jacoline B Ten Brink; Frans P M Cremers; Alberta A H J Thiadens; L Ingeborgh van den Born; Carel B Hoyng; Magda A Meester-Smoor; Arthur A Bergen; Camiel J F Boon
Journal:  Acta Ophthalmol       Date:  2021-02-02       Impact factor: 3.761

7.  Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa.

Authors:  Muhammad Ajmal; Muhammad Imran Khan; Shazia Micheal; Waqas Ahmed; Ashfa Shah; Hanka Venselaar; Habib Bokhari; Aisha Azam; Nadia Khalida Waheed; Rob W J Collin; Anneke I den Hollander; Raheel Qamar; Frans P M Cremers
Journal:  Mol Vis       Date:  2012-05-10       Impact factor: 2.367

8.  Targeted disruption of outer limiting membrane junctional proteins (Crb1 and ZO-1) increases integration of transplanted photoreceptor precursors into the adult wild-type and degenerating retina.

Authors:  R A Pearson; A C Barber; E L West; R E MacLaren; Y Duran; J W Bainbridge; J C Sowden; R R Ali
Journal:  Cell Transplant       Date:  2010-01-20       Impact factor: 4.064

9.  A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.

Authors:  Leila Tiab; Leila Largueche; Ibtissem Chouchane; Kaouthar Derouiche; Francis L Munier; Leila El Matri; Daniel F Schorderet
Journal:  Mol Vis       Date:  2013-04-05       Impact factor: 2.367

10.  High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population.

Authors:  Marta Corton; Sorina D Tatu; Almudena Avila-Fernandez; Elena Vallespín; Ignacio Tapias; Diego Cantalapiedra; Fiona Blanco-Kelly; Rosa Riveiro-Alvarez; Sara Bernal; Blanca García-Sandoval; Montserrat Baiget; Carmen Ayuso
Journal:  Orphanet J Rare Dis       Date:  2013-02-05       Impact factor: 4.123

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