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

Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Jan 1998

Cunningham E T, Eliott D, Miller N R, Maumenee I H, Green W R

Abstract excerpt

OBJECTIVE: To describe the clinical and ocular histopathological findings in multiple members of a family with congenital Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss. METHODS: We performed a retrospective review of the medical charts and the ocular histopathological material of multiple members of a family. RESULTS: Congenital Axenfeld-Rieger anomaly and glaucoma were inherited...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Eye Abnormalities

Share to Hearing Loss, Sensorineural

Share to Infant

Share to Pedigree

Share to Phenotype

Share to Syndrome

Source

Identifiers

PMID: 9445211
DOI: 10.1001/archopht.116.1.78

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome.PMID 9445211Read ↗

Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?Semantic proximity Read ↗

Axenfeld-Rieger syndrome: new perspectives: Figure 1Semantic proximity Read ↗

Axenfeld-Rieger syndrome.Semantic proximity Read ↗

Axenfeld-Rieger syndrome in the age of molecular genetics.Semantic proximity Read ↗

Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and son.Semantic proximity Read ↗

Molecular genetics of Axenfeld-Rieger malformationsSemantic proximity Read ↗

A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings.Semantic proximity Read ↗

Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases.Semantic proximity Read ↗

Cardiac anomalies in Axenfeld-Rieger syndrome due to a novel FOXC1 mutation.Semantic proximity Read ↗

Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome).Semantic proximity Read ↗

Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld-anomaly in a child with PTPN11 mutation.Semantic proximity Read ↗

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.Semantic proximity Read ↗

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