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

Audiologic Features of Norrie Disease

1 Jul 2005

Abstract excerpt

OBJECTIVES: Norrie disease is an X-linked recessive disorder in which patients are born blind and develop sensory hearing loss in adolescence. The hearing loss associated with Norrie disease has been shown in a genetically altered knockout mouse to involve dysfunction of the stria vascularis; most other structures are preserved until the later stages of the disease. The objective of this study was to characterize...

Read the complete abstract on PubMed

Topics

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

Share to Hearing, Cochlea, Tinnitus, Genetics
Share to Ocular Disorders and Treatments
Share to Sympathectomy and Hyperhidrosis Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16134349
DOI: 10.1177/000348940511400707

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

Audiologic Features of Norrie DiseasePMID 16134349Read ↗

Vascular defects and sensorineural deafness in a mouse model of Norrie disease.Semantic proximity Read ↗

Norrie disease: extraocular clinical manifestations in 56 patients.Semantic proximity Read ↗

Twenty years of audiology in a patient with Norrie disease.Semantic proximity Read ↗

Auditory phenotype of DFNA17.Semantic proximity Read ↗

Auriculocondylar syndrome: Pathogenesis, clinical manifestations and surgical therapies.Semantic proximity Read ↗

Congenital hearing impairment.Semantic proximity Read ↗

A novel mutation in the Norrie disease gene.Semantic proximity Read ↗

Histopathology and molecular genetics of hearing loss in the human.Semantic proximity Read ↗

Auditory phenotype of DFNA1.Semantic proximity Read ↗

Using genetics to understand auditory function and improve diagnosis.Semantic proximity Read ↗

Anatomical Changes and Audiological Profile in Branchio-oto-renal Syndrome: A Literature ReviewSemantic proximity Read ↗

Characterization of Hearing-Impairment in Generalized Arterial Calcification of Infancy (GACI)Semantic proximity Read ↗

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