Erratum – Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Heshmati, Ali; Taghizadeh, Peyman; Ahmadieh, Hamid; Yaseri, Mehdi; Suri, Fatemeh; Alizadeh, M; Dadashzadeh, Marjan; Khatami, Hajar; Navi, Monireh Moradkhah; Zamanparvar, Parisa; Behboudi, Hassan; Elahi, Elahe

doi:10.18502/jovr.v17i2.10809

JOVR

2022

DOI: 10.18502/jovr.v17i2.10809

|View full text |Cite

Erratum – Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Ali Heshmati

Peyman Taghizadeh

Hamid Ahmadieh

et al.

Abstract: This is an Erratum to "Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran" [J Ophthalmic Vis Res 2021;16(4):574–581] and does not have an abstract. Please download the PDF or view the article HTML.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2023

Publication Types

Select...

Article1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 1 publication

References 0 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part I

Oganezova,

Kadyshev,

Egorov

2023

Oftalʹmologiâ

View full text Add to dashboard Cite

To understand the current situation with the genetic epidemiology of primary congenital glaucoma (PCG) in the world, as well as to identify genotype-phenotype correlations, 87 publications were analyzed from the Pubmed and elibrary databases, mainly the latest 5 years. This publication presents the first part of the analysis, covering Arab and African countries, Turkey, the USA, Brazil, Australia and New Zealand. The second part of the review, which will be published in early 2024, will focus on data from East and South Asia, Western Europe and Russia. The highest incidence of PCG is typical for Arab countries, which is associated with the presence of a significant number of consanguineous marriages in these countries. In most countries, boys predominated among patients with PCG, and the process was often bilateral. In Australia female patients predominate. The PCG phenotype is more severe in patients with CYP1B1 mutations (early onset, bilateral involvement) than in patients without mutations, and in patients with consanguineous parents than in children from unrelated marriages. Among the genetic causes of PCG in different populations, the most common (from 30 to 86 % of cases) in Arab countries, Brazil and Turkey are mutations in the CYP1B1 gene. The spectrum of mutations varies depending on the region. In Australia and New Zealand, biallelic mutations were identified in the CYP1B1, CPAMD8 and COL18A1 genes, as well as heterozygous mutations in the TEK, FOXC1 and ANGPT1. Mutations in rare genes were also found in patients with PCG from Lebanon (ANGPT1 (p.K186N), Mauritania (NTF4 (c.601T>G, p.Cys201Gly) and WDR36 (c.2078A>G, p.Asn693Ser)). In the USA, the influence of the thrombospondin gene (THBS1) on the development of PCG is being studied. Based on the results of genetic and epidemiological studies, specific treatment, rehabilitation and preventive programs can be developed, which will determine the success of PCG therapy in children, preserving their visual functions.

show abstract

Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part I

Oganezova,

Kadyshev,

Egorov

2023

Oftalʹmologiâ

View full text Add to dashboard Cite

show abstract

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Erratum – Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Abstract: This is an Erratum to "Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran" [J Ophthalmic Vis Res 2021;16(4):574–581] and does not have an abstract. Please download the PDF or view the article HTML.

Cited by 1 publication

References 0 publications

Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part I

Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part I

Contact Info

Product

Resources

About