Literature DB >> 16735991

Further support of the role of CYP1B1 in patients with Peters anomaly.

Andrea Vincent1, Gail Billingsley, Megan Priston, Tom Glaser, Edward Oliver, Mike Walter, Robert Ritch, Alex Levin, Elise Heon.   

Abstract

PURPOSE: Peters anomaly is a developmental anomaly of the eye frequently associated with glaucoma. The aim of this study was to further define the molecular basis of this condition.
METHODS: The role of four candidate genes implicated in ocular development or glaucoma, PAX6, PITX2, MYOC, and CYP1B1, was studied in 15 patients with Peters anomaly. Mutational analysis used a combination of single strand conformation polymorphism (SSCP) and direct cycle sequencing.
RESULTS: Four mutations in CYP1B1 were found in 3/15 (20%) affected individuals compared with 1/140 (0.7%) control individuals.
CONCLUSIONS: This study supports the role of CYP1B1 as a causative gene in Peters anomaly. Furthermore, this emphasizes the broad range of phenotypic expression for CYP1B1 mutations, and its role in eye development.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16735991

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  18 in total

1.  Carrier frequency of CYP1B1 mutations in the United States (an American Ophthalmological Society thesis).

Authors:  Janey L Wiggs; Anne M Langgurth; Keri F Allen
Journal:  Trans Am Ophthalmol Soc       Date:  2014-07

2.  Mutation spectrum of the CYP1B1 gene for congenital glaucoma in the Japanese population.

Authors:  Nobuo Fuse; Akiko Miyazawa; Kana Takahashi; Michiru Noro; Toru Nakazawa; Kohji Nishida
Journal:  Jpn J Ophthalmol       Date:  2010-02-12       Impact factor: 2.447

Review 3.  Genetics of anterior segment dysgenesis disorders.

Authors:  Linda M Reis; Elena V Semina
Journal:  Curr Opin Ophthalmol       Date:  2011-09       Impact factor: 3.761

4.  Whole exome sequence analysis of Peters anomaly.

Authors:  Eric Weh; Linda M Reis; Hannah C Happ; Alex V Levin; Patricia G Wheeler; Karen L David; Erin Carney; Brad Angle; Natalie Hauser; Elena V Semina
Journal:  Hum Genet       Date:  2014-09-03       Impact factor: 4.132

Review 5.  Ocular cytochrome P450s and transporters: roles in disease and endobiotic and xenobiotic disposition.

Authors:  Mariko Nakano; Catherine M Lockhart; Edward J Kelly; Allan E Rettie
Journal:  Drug Metab Rev       Date:  2014-05-26       Impact factor: 4.518

6.  A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.

Authors:  Lance Doucette; Jane Green; Bridget Fernandez; Gordon J Johnson; Patrick Parfrey; Terry-Lynn Young
Journal:  Eur J Hum Genet       Date:  2010-12-08       Impact factor: 4.246

Review 7.  Primary congenital and developmental glaucomas.

Authors:  Carly J Lewis; Adam Hedberg-Buenz; Adam P DeLuca; Edwin M Stone; Wallace L M Alward; John H Fingert
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

8.  Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.

Authors:  Ivan Prokudin; Cas Simons; John R Grigg; Rebecca Storen; Vikrant Kumar; Zai Y Phua; James Smith; Maree Flaherty; Sonia Davila; Robyn V Jamieson
Journal:  Eur J Hum Genet       Date:  2013-11-27       Impact factor: 4.246

9.  Axenfeld-Rieger Syndrome Associated with Congenital Glaucoma and Cytochrome P4501B1 Gene Mutations.

Authors:  Mukesh Tanwar; Tanuj Dada; Rima Dada
Journal:  Case Rep Med       Date:  2010-08-09

10.  Two sisters with microphthalmia and anterior segment dysgenesis secondary to a PAX6 pathogenic variant with clinically healthy parents: a case of gonadal mosaicism?

Authors:  Anna Wawrocka; Joanna Walczak-Sztulpa; Ewelina Bukowska-Olech; Aleksander Jamsheer; Marcin Jaworski; Piotr Jaworski; Maciej Robert Krawczynski
Journal:  Jpn J Ophthalmol       Date:  2020-02-03       Impact factor: 2.447

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.