Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

Journal of glaucoma - 1 Jan 2007

El-Ashry Mohamed F, Abd El-Aziz Mai M, Bhattacharya Shomi S

Abstract excerpt

PURPOSE: To undertake mutation screening of cytochrome P4501B1 (CYP1B1, OMIM 601771) and myocilin (MYOC, OMIM 601652) genes in Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG). PATIENTS AND METHODS: A clinical and molecular genetic study was performed on 11 Egyptian and Saudi Arabian patients with PCG. Clinical diagnosis was confirmed by slit lamp biomicroscopy, gonioscopy, measurement...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Saudi Arabia
Share to Aryl Hydrocarbon Hydroxylases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Consanguinity

Share to Cytochrome P-450 CYP1B1

Share to Glaucoma

Share to Intraocular Pressure

Share to Molecular Biology

Source

Identifiers

PMID: 17224759
DOI: 10.1097/01.ijg.0000212288.00917.e1

Genes

MYOC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).PMID 17224759Read ↗

A clinical and molecular genetics study of primary congenital glaucoma in South Korea.Semantic proximity Read ↗

Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma.Semantic proximity Read ↗

CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.Semantic proximity Read ↗

Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.Semantic proximity Read ↗

Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.Semantic proximity Read ↗

CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients.Semantic proximity Read ↗

Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review.Semantic proximity Read ↗

CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma.Semantic proximity Read ↗

Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.Semantic proximity Read ↗

Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital GlaucomaSemantic proximity Read ↗

Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients.Semantic proximity Read ↗

Genetic analysis of patients with primary congenital glaucoma.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.